IP Library › Granted Patent US 10,336,762
Granted Patent B2
US 10,336,762 · App. 15/898,095 · Granted Jul 2, 2019

Pyrrolo[1,2-b]pyridazine derivatives

Inventors: Elizabeth M. Bacon (Burlingame, CA); Gediminas Brizgys (Menlo Park, CA); Elbert Chin (San Mateo, CA); Chienhung Chou (Dublin, CA); Jeromy J. Cottell (Redwood City, CA); John O. Link (San Francisco, CA); James G. Taylor (Burlingame, CA); Winston C. Tse (Redwood City, CA); Nathan E. Wright (Foster City, CA); Zheng-Yu Yang (Palo Alto, CA); Jennifer R. Zhang (Union City, CA); Sheila M. Zipfel (San Mateo, CA)
Assignee: Gilead Sciences, Inc.
C07D487/04A61P29/00C07D453/00C07D519/00
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Quick Facts
Patent No.
US 10,336,762
App. No.
15/898,095
Granted
Jul 2, 2019
Kind
B2
Abstract

Provided is a compound of Formula (I) wherein the variable groups are defined herein.

Claims (367)

1. A compound of Formula (I)

wherein:

R 1 and R 2 are each independently selected from:

a) C 1-10 alkyl optionally substituted with Z 1 ;

b) C 3-10 cycloalkyl optionally substituted with Z 1 ;

c) 5-10 membered heteroaryl optionally substituted with Z 1 ;

d) C 6-10 aryl optionally substituted with Z 1 ;

e) 4-7 membered monocyclic heterocyclyl optionally substituted with Z 1 ;

f) 6-12 membered bicyclic heterocyclyl optionally substituted with Z 1 ; or

g) —N(R 12 )(R 12 ), —S(O) 2 R 12 , —S(O) 2 N(R 12 )(R 12 ), or —H;

R 3 and R 4 are each independently selected from:

a) H, halo, —NO 2 , —CN, —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )C(O)—N(R 12 )(R 12 ), —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

b) C 1-9 alkyl optionally substituted with Z 1 ;

c) C 2-9 alkynyl optionally substituted with Z 1 ;

d) C 2-9 alkenyl optionally substituted with Z 1 ;

e) 5-10 membered heteroaryl optionally substituted with Z 1 ;

f) C 6-10 aryl optionally substituted with Z 1 ;

g) 4-12 membered heterocyclyl optionally substituted with Z 1 ; or

h) C 3-10 cycloalkyl optionally substituted with Z 1 ;

R 5 , R 6 and R 7 are each independently selected from:

a) H, halo, —NO 2 , —CN, —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , or —N(R 12 )S(O) 2 (R 12 ;

b) C 1-5 alkyl optionally substituted with Z 1 ; or

c) Cyclopropyl, oxetanyl or azetidinyl optionally substituted with Z 1 ;

Z 1 is independently oxo, halo, —NO 2 , —N 3 , —CN, C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1a ;

each Z 1a is independently oxo, halo, —NO 2 , —CN, —N 3 , C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1b ;

each R 12 is independently H, C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl or heterocyclyl;

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1a ;

each Z 1b is independently oxo, hydroxy, halo, —NO 2 , —N 3 , —CN, C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —O(C 1-9 alkyl), —O(C 2-6 alkenyl), —O(C 2-6 alkynyl), —O(C 3-15 cycloalkyl), —O(C 1-8 haloalkyl), —O(aryl), —O(heteroaryl), —O(heterocyclyl), —NH 2 , —NH(C 1-9 alkyl), —NH(C 2-6 alkenyl), —NH(C 2-6 alkynyl), —NH(C 3-15 cycloalkyl), —NH(C 1-8 haloalkyl), —NH(aryl), —NH(heteroaryl), —NH(heterocyclyl), —N(C 1-9 alkyl) 2 , —N(C 3-15 cycloalkyl) 2 , —N(C 2-6 alkenyl) 2 , —N(C 2-6 alkynyl) 2 , —N(C 3-15 cycloalkyl) 2 , —N(C 1-8 haloalkyl) 2 , —N(aryl) 2 , —N(heteroaryl) 2 , —N(heterocyclyl) 2 , —N(C 1-9 alkyl)(C 3-15 cycloalkyl), —N(C 1-9 alkyl)(C 2-6 alkenyl), —N(C 1-9 alkyl)(C 2-6 alkynyl), —N(C 1-9 alkyl)(C 3-15 cycloalkyl), —N(C 1-9 alkyl)(C 1-8 haloalkyl), —N(C 1-9 alkyl)(aryl), —N(C 1-9 alkyl)(heteroaryl), —N(C 1-9 alkyl)(heterocyclyl), —C(O)(C 1-9 alkyl), —C(O)(C 2-6 alkenyl), —C(O)(C 2-6 alkynyl), —C(O)(C 3-15 cycloalkyl), —C(O)(C 1-8 haloalkyl), —C(O)(aryl), —C(O)(heteroaryl), —C(O)(heterocyclyl), —C(O)O(C 1-9 alkyl), —C(O)O(C 2-6 alkenyl), —C(O)O(C 2-6 alkynyl), —C(O)O(C 3-15 cycloalkyl), —C(O)O(C 1-8 haloalkyl), —C(O)O(aryl), —C(O)O(heteroaryl), —C(O)O(heterocyclyl), —C(O)NH 2 , —C(O)NH(C 1-9 alkyl), —C(O)NH(C 2-6 alkenyl), —C(O)NH(C 2-6 alkynyl), —C(O)NH(C 3-15 cycloalkyl), —C(O)NH(C 1-8 haloalkyl), —C(O)NH(aryl), —C(O)NH(heteroaryl), —C(O)NH(heterocyclyl), —C(O)N(C 1-9 alkyl) 2 , —C(O)N(C 3-15 cycloalkyl) 2 , —C(O)N(C 2-6 alkenyl) 2 , —C(O)N(C 2-6 alkynyl) 2 , —C(O)N(C 3-15 cycloalkyl) 2 , —C(O)N(C 1-8 haloalkyl) 2 , —C(O)N(aryl) 2 , —C(O)N(heteroaryl) 2 , —C(O)N(heterocyclyl) 2 , —NHC(O)(C 1-9 alkyl), —NHC(O)(C 2-6 alkenyl), —NHC(O)(C 2-6 alkynyl), —NHC(O)(C 3-15 cycloalkyl), —NHC(O)(C 1-8 haloalkyl), —NHC(O)(aryl), —NHC(O)(heteroaryl), —NHC(O)(heterocyclyl), —NHC(O)O(C 1-9 alkyl), —NHC(O)O(C 2-6 alkenyl), —NHC(O)O(C 2-6 alkynyl), —NHC(O)O(C 3-15 cycloalkyl), —NHC(O)O(C 1-8 haloalkyl), —NHC(O)O(aryl), —NHC(O)O(heteroaryl), —NHC(O)O(heterocyclyl), —NHC(O)NH(C 1-9 alkyl), —NHC(O)NH(C 2-6 alkenyl), —NHC(O)NH(C 2-6 alkynyl), —NHC(O)NH(C 3-15 cycloalkyl), —NHC(O)NH(C 1-8 haloalkyl), —NHC(O)NH(aryl), —NHC(O)NH(heteroaryl), —NHC(O)NH(heterocyclyl), —SH, —S(C 1-9 alkyl), —S(C 2-6 alkenyl), —S(C 2-6 alkynyl), —S(C 3-15 cycloalkyl), —S(C 1-8 haloalkyl), —S(aryl), —S(heteroaryl), —S(heterocyclyl), —NHS(O)(C 1-9 alkyl), —N(C 1-9 alkyl)(S(O)(C 1-9 alkyl), —S(O)N(C 1-9 alkyl) 2 , —S(O)(C 1-9 alkyl), —S(O)(NH)(C 1-9 alkyl), —S(O)(C 2-6 alkenyl), —S(O)(C 2-6 alkynyl), —S(O)(C 3-15 cycloalkyl), —S(O)(C 1-8 haloalkyl), —S(O)(aryl), —S(O)(heteroaryl), —S(O)(heterocyclyl), —S(O) 2 (C 1-9 alkyl), —S(O) 2 (C 2-6 alkenyl), —S(O) 2 (C 2-6 alkynyl), —S(O) 2 (C 3-15 cycloalkyl), —S(O) 2 (C 1-8 haloalkyl), —S(O) 2 (aryl), —S(O) 2 (heteroaryl), —S(O) 2 (heterocyclyl), —S(O) 2 NH(C 1-9 alkyl), or —S(O) 2 N(C 1-9 alkyl) 2 ;

wherein any alkyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with one or more halo, C 1-9 alkyl, C 1-8 haloalkyl, —OH, —NH 2 , —NH(C 1-9 alkyl), —NH(C 3-15 cycloalkyl), —NH(C 1-8 haloalkyl), —NH(aryl), —NH(heteroaryl), —NH(heterocyclyl), —N(C 1-9 alkyl) 2 , —N(C 3-15 cycloalkyl) 2 , —NHC(O)(C 3-15 cycloalkyl), —NHC(O)(C 1-8 haloalkyl), —NHC(O)(aryl), —NHC(O)(heteroaryl), —NHC(O)(heterocyclyl), —NHC(O)O(C 1-9 alkyl), —NHC(O)O(C 2-6 alkynyl), —NHC(O)O(C 3-15 cycloalkyl), —NHC(O)O(C 1-8 haloalkyl), —NHC(O)O(aryl), —NHC(O)O(heteroaryl), —NHC(O)O(heterocyclyl), —NHC(O)NH(C 1-9 alkyl), —S(O)(NH)(C 1-9 alkyl), S(O) 2 (C 1-9 alkyl), —S(O) 2 (C 3-15 cycloalkyl), —S(O) 2 (C 1-8 haloalkyl), —S(O) 2 (aryl), —S(O) 2 (heteroaryl), —S(O) 2 (heterocyclyl), —S(O) 2 NH(C 1-9 alkyl), —S(O) 2 N(C 1-9 alkyl) 2 , —O(C 3-15 cycloalkyl), —O(C 1-8 haloalkyl), —O(aryl), —O(heteroaryl), —O(heterocyclyl), or —O(C 1-9 alkyl); and

with the proviso that when R 1 is C 3 alkyl, R 2 is C 5 alkyl substituted with F and hydroxyl, R 3 , R 5 , R 6 , R 7 are H, and R 4 is CN, then R 1 is substituted with oxo, halo, —NO 2 , —N 3 , —CN, C 2-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1a ;

or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof.

2. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 1-10 alkyl optionally substituted with Z 1 , with the proviso that when R 1 is C 3 alkyl, R 2 is C 5 alkyl substituted with F and hydroxyl, R 3 , R 5 , R 6 , R 7 are H, and R 4 is CN, then R 1 is substituted with oxo, halo, —NO 2 , —N 3 , —CN, C 2-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, aryl, heteroaryl or 4-20 membered heterocyclyl is optionally substituted with Z 1a .

3. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is methyl.

4. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is C 6-10 alkyl optionally substituted with Z 1 .

5. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 1-5 alkyl substituted with one or more substituents selected from —Cl, oxo, —CN, C 2-6 alkenyl, C 2-6 alkynyl, cyclopropyl, naphthyl, heteroaryl, nitrogen or sulfur containing monocyclic 4-20 membered heterocyclyl, bicyclic 4-20 membered heterocyclyl, C 7-15 cycloalkyl, —O—R 9 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

R 9 at each occurrence is independently C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 haloalkyl, C 3-15 cycloalkyl, aryl, 4-20 membered heterocyclyl, or heteroaryl;

wherein each C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 haloalkyl, C 3-15 cycloalkyl, aryl, heterocyclyl, or heteroaryl is optionally substituted with Z 1a ;

wherein said C 1-5 alkyl is also optionally substituted with Z 1 ; and

wherein each said C 2-6 alkenyl, C 2-6 alkynyl, cyclopropyl, naphthyl, heteroaryl, nitrogen or sulfur containing monocyclic 4-20 heterocyclyl, bicyclic 4-20 heterocyclyl, or C 7-15 cycloalkyl is optionally substituted with Z 1a .

6. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 1-5 alkyl optionally substituted with Z 1 ;

wherein said C 1-5 alkyl is substituted with one or more C 4-6 cycloalkyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, or phenyl;

wherein said C 4-6 cycloalkyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, or phenyl is optionally substituted with Z 1a ;

wherein said C 4-6 cycloalkyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, or phenyl is substituted by one or more halo, oxo, —CN, C 2-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-7 cycloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) +, —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and wherein said C 2-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-7 cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1b .

7. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 1-5 alkyl optionally substituted with F or —OH and substituted with one or more substituents selected from C 4-6 cycloalkyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, or phenyl; wherein said C 4-6 cycloalkyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, or phenyl is substituted with two or more substituents selected from —OH and —CH 3 and optionally substituted with Z 1a .

8. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is C 3-10 cycloalkyl optionally substituted with Z 1 .

9. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 7-10 cycloalkyl optionally substituted with Z 1 , wherein when said C 7 -C 10 cycloalkyl is bicyclo[2.2.1]heptanyl, then said C 7-10 cycloalkyl is substituted with at least one of oxo, —Cl, —NO 2 , —CN, —N 3 , C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 7-15 cycloalkyl, C 5-8 haloalkyl, aryl, pyrazolyl, —O—R 9 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , or —S(O) 2 N(R 12 )(R 12 ).

10. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 3-6 cycloalkyl substituted with one or more —O—R 16 ;

wherein said C 3-6 cycloalkyl is optionally substituted with Z 1 ;

R 16 at each occurrence is independently C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 haloalkyl, C 3-15 cycloalkyl, aryl, 4-20 membered heterocyclyl, or heteroaryl;

wherein each C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 haloalkyl, C 3-15 cycloalkyl, aryl, heterocyclyl, or heteroaryl is optionally substituted with Z 1a .

11. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 3-6 cycloalkyl substituted with one or more —C(O)—R 11 ;

wherein said C 3-6 cycloalkyl is optionally substituted with Z 1 ;

wherein R 11 at each occurrence is independently C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, 4-20 membered heterocyclyl, or heteroaryl,

wherein each C 1-9 alkyl is optionally substituted with —NO 2 , —N 3 , —CN, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 4-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein each said C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heterocyclyl, or heteroaryl is optionally substituted with Z 1a .

12. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 3-6 cycloalkyl substituted with one or more oxo, C 5-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —C(O)O—R 12 , —C(O)—N(R 9 )(R 9 ), —C(O)N(H)(C 4-9 alkyl), —C(O)N(H)(C 3-10 cycloalkyl), —C(O)N(H)(4-20 membered heterocyclyl), —C(O)N(H)(aryl), —C(O)N(H)(heteroaryl), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 5-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl, heterocyclyl, —C(O)N(H)(C 4-9 alkyl), —C(O)N(H)(C 3-10 cycloalkyl), —C(O)N(H)(4-20 membered heterocyclyl), —C(O)N(H)(aryl), or —C(O)N(H)(heteroaryl) is optionally substituted with Z 1a ; and wherein said C 3-6 cycloalkyl is optionally substituted with Z 1 ;

wherein when C 3-6 cycloalkyl is bicyclo[1.1.1]pentanyl; then said bicyclo[1.1.1]pentanyl is substituted with one or more oxo, —NO 2 , —N 3 , C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 7-15 cycloalkyl, C 5-8 haloalkyl, aryl, pyrazolyl, —O—R 16 , —C(O)R 1 , —C(O)O—R 12 , —C(O)N(R 9 )(R 9 ), —C(O)N(H)(C 4 alkyl), —C(O)N(H)(R 16 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , or —S(O) 2 N(R 12 )(R 12 ).

13. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein

R 1 is C 3-6 cycloalkyl substituted with C 4 alkyl, wherein said C 4 alkyl is optionally substituted with halo, —NO 2 , —CN, —N 3 , C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1a ; and

wherein said C 3-6 cycloalkyl is optionally substituted with Z 1 ;

wherein when said C 3-6 cycloalkyl is bicyclo[1.1.1]pentanyl substituted with C 4 alkyl then said C 4 alkyl is further substituted with oxo, —NO 2 , —N 3 , C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 7-15 cycloalkyl, C 5-8 haloalkyl, aryl, heteroaryl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , or —S(O) 2 N(R 12 )(R 12 ).

14. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is C 3-6 cycloalkyl optionally substituted with Z 1 ; and

wherein said C 3-6 cycloalkyl is substituted with four or more substituents selected from the group consisting of F, —OH, —Cl, —CN, C 1-3 alkyl, C 1-3 fluoroalkyl, C 1-4 hydroxyalkyl, C 1-4 alkoxy, —C(O)NH 2 , —C(O)NH(C 1-3 alkyl); and —C(O)(C 1-3 fluoroalkyl).

15. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 3-6 cycloalkyl substituted with C 1-3 fluoroalkyl, or —C(O)(C 1-3 fluoroalkyl)

wherein said C 3-6 cycloalkyl is also optionally substituted with Z 1 ;

wherein said C 1-3 fluoroalkyl or —C(O)(C 1-3 fluoroalkyl) is further substituted with at least one oxo, —Cl, —NO 2 , —CN, —N 3 , C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 3-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 3-8 haloalkyl, aryl, heteroaryl, heterocyclyl is optionally substituted with Z 1b .

16. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 3-6 cycloalkyl substituted with at least one C 1-3 alkyl or C 1-4 hydroxyalkyl wherein said C 3-6 cycloalkyl is optionally substituted with Z 1 ;

wherein said C 1-3 alkyl or C 1-4 hydroxyalkyl is further substituted with oxo, chloro, —NO 2 , —CN, —N 3 , C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl is optionally substituted with Z 1b .

17. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is C 3-6 cycloalkyl substituted with at least one C 1-4 alkoxy or C(O)NH(C 1-3 alkyl);

wherein said C 3-6 cycloalkyl is optionally substituted with Z 1 and wherein said C 1-4 alkoxy or C(O)NH(C 1-3 alkyl) is further substituted with oxo, halo, —NO 2 , —CN, —N 3 , C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 2 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl is optionally substituted with Z 1b .

18. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is 5-10 membered heteroaryl optionally substituted with Z 1 .

19. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is imidazolyl, triazolyl, oxazolyl, isoxazolyl, pyridinyl, thiadiazole, oxadiazole, pyrimidinyl, pyridizinyl, pyrazinyl, isothiazolyl, tetrazolyl, thiophenyl, furanyl, triazinyl, or 8-10 membered heteroaryl optionally substituted with Z 1 .

20. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is a 6 membered heteroaryl optionally substituted with Z 1 .

21. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is 4-7 membered monocyclic heterocyclyl optionally substituted with Z 1 .

22. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is azetidinyl, morpholinyl, thiomorpholinyl, 4-7 membered sultam, 4-7 membered cyclic carbamate, 4-7 membered cyclic carbonate, or 4-7 membered cyclic sulfide optionally substituted with Z 1 .

23. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is 6-12 membered bicyclic heterocyclyl optionally substituted with Z 1 ;

wherein when said 6-12 membered bicyclic heterocyclyl is 4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazinyl then said 6-12 membered bicyclic heterocyclyl is substituted with at least one oxo, C 3-6 cycloalkyl, or C(O)(C 1-5 alkyl).

24. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl, or thiazolyl;

wherein said oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl or thiazolyl, is substituted with one or more substituents selected from —Cl, oxo, —CN, C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 7-10 cycloalkyl, aryl, pyridinyl, pyridizinyl, 5-10 membered bicyclic heteroaryl, 5-membered heteroaryl, nitrogen or sulfur containing monocyclic 4-20 membered heterocyclyl, bicyclic heterocyclyl, —O—R 9 , —C(O)—R 11 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , or —S(O) 2 N(R 12 )(R 12 );

wherein said C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 7-10 cycloalkyl, aryl, pyridinyl, pyridizinyl, 5-10 membered bicyclic heteroaryl, 5-membered heteroaryl, nitrogen or sulfur containing monocyclic heterocyclyl or bicyclic 4-10 membered heterocyclyl is optionally substituted with Z 1a ;

wherein said oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl, thiazolyl, is optionally substituted with Z 1 .

25. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl, or thiazolyl;

wherein said oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl, or thiazolyl, is optionally substituted with Z 1 ;

wherein said oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl, thiazolyl, is substituted with 3 or more substituents selected from F, —OH, C 1-4 alkyl, C 1-3 hydroxyalkyl, C 1-4 fluoroalkyl, —(CH 2 ) 1-3 O(C 1-3 alkyl), —C(O)(C 1-3 fluoroalkyl), —S(O) 2 (C 1-3 alkyl), C 3-6 cycloalkyl, C 3-6 fluorocycloalkyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrimidinyl, fluoropyrimidinyl, or methoxyprimidinyl.

26. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein

R 1 is pyrrolidinyl, piperidinyl, pyrazolyl or thiazolyl;

wherein said pyrrolidinyl, piperidinyl, pyrazolyl or thiazolyl is optionally substituted with Z 1 ;

wherein said pyrrolidinyl, piperidinyl, pyrazolyl or thiazolyl is substituted with one or more substituents independently selected from —(CH 2 ) 1-3 O(C 1-3 alkyl), —S(O) 2 (C 1-3 alkyl), oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, or CH 2 (C 3-6 cycloalkyl); and

wherein said —(CH 2 ) 1-3 O(C 1-3 alkyl), —S(O) 2 (C 1-3 alkyl), oxetanyl, tetrahydrofuranyl, tetrahydropyranyl or CH 2 (C 3-6 cycloalkyl) are independently substituted with one or more oxo, halo, —NO 2 , —CN, —N 3 , C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1b .

27. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl, or thiazolyl; wherein said oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl, or thiazolyl is optionally substituted with a —F or —OH and is substituted with one or more substituents independently selected from C 1-4 alkyl or C 1-3 hydroxyalkyl;

wherein said C 1-4 alkyl or C 1-3 hydroxyalkyl is substituted with one or more oxo, —Cl, —NO 2 , —CN, —N 3 , C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 7-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 16 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein any alkyl, hydroxyalkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1b .

28. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl, or thiazolyl;

wherein said oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, piperidinyl, pyrazolyl, or thiazolyl is optionally substituted with a —F or —OH and is substituted with one or more substituents independently selected from C 1-4 fluoroalkyl, —C(O)(C 1-3 fluoroalkyl), C 3-6 cycloalkyl, C 3-6 fluorocycloalkyl, and fluoropyrimidinyl;

wherein said C 1-4 fluoroalkyl, —C(O)(C 1-3 fluoroalkyl), C 3-6 cycloalkyl, C 3-6 fluorocycloalkyl or fluoropyrimidyl is substituted with one or more oxo, —Cl, —NO 2 , —CN, —N 3 , C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1b .

29. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is C 6-10 aryl optionally substituted with Z 1 .

30. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 6-10 aryl is substituted with one or more C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 11 , —C(O)O—R 12 , —C(O)NH(C 3-6 cycloalkyl), —C(O)NH(C 4-6 alkyl), —C(O) 4-20 membered heterocyclyl, N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl, heterocyclyl, —C(O)NH(C 3-6 cycloalkyl), —C(O)NH(C 4-6 alkyl),or —C(O) 4-20 membered heterocyclyl is optionally substituted with Z 1a ;

wherein said C 6-10 aryl is optionally substituted with Z 1 .

31. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 6-10 aryl substituted with one or more —C(O)NH(C 1-3 alkyl) and optionally substituted with Z 1a ;

wherein said —C(O)NH(C 1-3 alkyl) is substituted with one or more oxo, halo, —NO 2 , —CN, —N 3 , C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1b .

32. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 1 is C 6-10 aryl substituted with one or more —C(O)(C 1-3 fluoroalkyl);

wherein said —C(O)(C 1-3 fluoroalkyl) is substituted with one or more oxo, —Cl, —NO 2 , —CN, —N 3 , C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 3-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 3-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1b ; and

wherein said C 6-10 aryl is optionally substituted with Z 1 .

33. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is —N(R 12 )(R 12 ), —S(O) 2 R 12, —S(O) 2 N(R 12 )(R 12 ), or —H.

34. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is C 1-10 alkyl optionally substituted with Z 1 .

35. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is C 1-10 alkyl.

36. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is C 7-10 alkyl, optionally substituted with Z 1 .

37. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 1-6 alkyl substituted with one or more —O(C 1-2 alkyl), —NHC(O)(C 1-3 alkyl), or —S(O) 2 (C 1-3 alkyl);

wherein said —O(C 1-2 alkyl) is substituted with one or more oxo, —Cl, —NO 2 , —CN, —N 3 , C 2-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 2-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and said —O(C 1-2 alkyl) is optionally substituted with —F;

wherein said —NHC(O)(C 1-3 alkyl), or —S(O) 2 (C 1-3 alkyl) is substituted with one or more oxo, halo, —NO 2 , —CN, —N 3 , C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 1-6 alkyl is optionally substituted with Z 1a ; and

wherein each said C 2-9 alkyl, C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, C 2-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1b .

38. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 4-6 alkyl substituted with one or more substituents selected from —Cl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl, monocyclic 4-20 membered heterocyclyl, 4-10 membered bicyclic heterocyclyl, —O(C 3-9 alkyl), —O(C 3-10 cycloalkyl), —O(4-20 membered heterocyclyl), —O(aryl), —O(heteroaryl), —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)(C 4-9 alkyl), —N(R 12 )C(O)(C 3-10 cycloalkyl), —N(R 12 )C(O)(4-20 membered heterocyclyl), —N(R 12 )C(O)(aryl), —N(R 12 )C(O)(heteroaryl), —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 (C 4-9 alkyl), —S(O) 2 (aryl), —S(O) 2 (C 3-10 cycloalkyl), —S(O) 2 (4-20 membered heterocyclyl), —S(O) 2 (heteroaryl), or —S(O) 2 N(R 12 )(R 12 );

wherein said C 4-6 alkyl is also optionally substituted with Z 1 ; and

wherein said C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl, monocyclic 4-20 membered heterocyclyl, bicyclic 4-10 membered heterocyclyl, —O(C 3-9 alkyl), —O(C 3-10 cycloalkyl), —O(4-20 membered heterocyclyl), —O(aryl), —O(heteroaryl), —N(R 12 )C(O)(C 4-9 alkyl), —N(R 12 )C(O)(C 3-10 cycloalkyl), —N(R 12 )C(O)(4-20 membered heterocyclyl), —N(R 12 )C(O)(aryl), —N(R 12 )C(O)(heteroaryl), —S(O) 2 (C 4-9 alkyl), —S(O) 2 (aryl), —S(O) 2 (C 3-10 cycloalkyl), —S(O) 2 (4-20 membered heterocyclyl), —S(O) 2 (heteroaryl), —NHC(O)(C 1-3 alkyl), or —S(O) 2 (C 1-3 alkyl) is optionally substituted with Z 1a .

39. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 4-6 alkyl substituted with one or more —O(CH 2 ) 2 R 17 or —O(CH 2 )R 17 ;

R 17 at each occurrence is independently C 3-15 cycloalkyl, aryl, 4-20 membered heterocyclyl, heteroaryl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 3-15 cycloalkyl, aryl, heterocyclyl, and heteroaryl optionally is substituted with Z 1b ; and

wherein said C 4-6 alkyl is also optionally substituted with Z 1 .

40. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 4-6 alkyl substituted with five or more substituents selected from F, hydroxyl, —CN, —OCH 3 , —OCD 3 , —NHC(O)(C 1-3 alkyl), —S(O) 2 (C 1-3 alkyl), or C 1-2 fluoroalkoxy; and

wherein said C 4-6 alkyl is optionally substituted with Z 1 .

41. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 1-3 alkyl substituted with one or more substituents selected from —Cl, C 2-6 alkenyl, C 2-6 alkynyl, cyclopropyl, napthyl, bicyclic 4-10 membered heterocyclyl, C 7-15 cycloalkyl, —O(CH 2 ) 2 R 17 , —O(CH 2 )R 17 , —O(C 3-9 alkyl), —O(C 3-10 cycloalkyl), —O(4-20 membered heterocyclyl), —O(aryl), —O(heteroaryl), —C(O)(C 1-9 alkyl), —C(O)(cyclopropyl), —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)(C 4-9 alkyl), —N(R 12 )C(O)(C 3-10 cycloalkyl), —N(R 12 )C(O)(4-20 membered heterocyclyl), —N(R 12 )C(O)(aryl), —N(R 12 )C(O)(heteroaryl), —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 (C 4-9 alkyl), —S(O) 2 (aryl), —S(O) 2 (C 3-10 cycloalkyl), —S(O) 2 (4-20 membered heterocyclyl), —S(O) 2 (heteroaryl), or —S(O) 2 N(R 9 )(R 12 );

wherein said C 1-3 alkyl is also optionally substituted with Z 1 ; and

wherein said C 2-6 alkenyl, C 2-6 alkynyl, cyclopropyl, napthyl, bicyclic heterocyclyl, C 7-15 cycloalkyl, —O(C 3-9 alkyl), —O(C 3-10 cycloalkyl), —O(heterocyclyl), —O(aryl), —O(heteroaryl), —N(R 12 )C(O)(C 4-9 alkyl), —N(R 12 )C(O)(C 3-10 cycloalkyl), —N(R 12 )C(O)(heterocyclyl), —N(R 12 )C(O)(aryl), —N(R 12 )C(O)(heteroaryl), —S(O) 2 (C 4-9 alkyl), —S(O) 2 (aryl), —S(O) 2 (C 3-10 cycloalkyl), —S(O) 2 (heterocyclyl), or —S(O) 2 (heteroaryl) is optionally substituted with Z 1a .

42. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 1-3 alkyl substituted with one or more substituents selected from azetidinyl, tetrahydrofuranyl, triazolyl, oxazolyl, isoxazolyl, thiadiazole, oxadiazole, pyrimidinyl, pyridizinyl, pyrazinyl, isothiazolyl, tetrazolyl, furanyl, thiomorpholinyl, 4-7 membered sultam, 4-7 membered cyclic carbamate, 4-7 membered cyclic carbonate, 4-7 membered cyclic sulfide, or 8-10 membered heteroaryl; any of which is optionally substituted with Z 1a ; and

wherein said C 1-3 alkyl is also optionally substituted with Z 1 .

43. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 1-3 alkyl substituted with one substituent selected from phenyl, oxetanyl, tetrahydropyranyl, morpholinyl, piperidinyl, imidazolyl, pyridinyl, thiophenyl, or C 4-6 cycloalkyl;

wherein said phenyl, oxetanyl, tetrahydropyranyl, morpholinyl, piperidinyl, imidazolyl, pyridinyl, thiophenyl, or C 4-6 cycloalkyl is substituted with one or more oxo, —NO 2 , —N 3 , —CN, C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O(C 3-6 alkyl), —O(C 3-6 cycloalkyl), —O(4-20 membered heterocyclyl), —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(O) O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 9 )(R 12 ); and

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1a .

44. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 1-3 alkyl optionally substituted with Z 1 and is substituted with one substituent selected from phenyl, oxetanyl, tetrahydropyranyl, morpholinyl, piperidinyl, imidazolyl, pyridinyl, thiophenyl, or C 4-6 cycloalkyl;

wherein said phenyl, oxetanyl, tetrahydropyranyl, morpholinyl, piperidinyl, imidazolyl, pyridinyl, thiophenyl, or C 4-6 cycloalkyl is substituted with four or more substituents selected from —F, —Cl, —OH, C 1-3 alkyl, —O(C 1-2 alkyl) or —S(O) 2 NH 2 .

45. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 1-3 alkyl substituted with oxo and optionally substituted with one or more substituents selected from halo, azetidinyl, pyrrolidinyl, piperazinyl, tetrahydrofuranyl, thiomorpholinyl, —CN, C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, cyclopropyl, C 7-15 cycloalkyl, C 1-8 haloalkyl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 9 )(R 12 ); and

wherein said C 1-3 alkyl is optionally substituted with Z 1 ;

wherein said, C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, cyclopropyl, C 7-15 cycloalkyl, C 1-8 haloalkyl, azetidinyl, pyrrolidinyl, piperazinyl, tetrahydrofuranyl, or thiomorpholinyl is optionally substituted with Z 1a .

46. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is C 3 alkyl substituted with five or more substituents selected from —F, —OH, —OCH 3 , —CN, —NHC(O)(C 1-3 alkyl), C 1-2 fluoroalkoxy, or —S(O) 2 (C 1-3 alkyl).

47. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is C 3-10 cycloalkyl optionally substituted with Z 1 .

48. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is cyclopropyl optionally substituted with Z 1 .

49. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is C 7-10 cycloalkyl optionally substituted with Z 1 .

50. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 4-6 cycloalkyl substituted with one or more substituents selected from -halo, oxo, —CN, C 1-4 alkyl, C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O(C 4-9 alkyl), —O(C 3-10 cycloalkyl), —O(4-20 membered heterocyclyl), —O(aryl), —O(heteroaryl), —N(R 12 )C(O)(C 5-9 alkyl), —N(R 12 )C(O)(C 3-10 cycloalkyl), —N(R 12 )C(O)(4-20 membered heterocyclyl), —N(R 12 )C(O)(aryl), —N(R 12 )C(O)(4-20 membered heteroaryl), —NH(R 12 ), —N(R 12 )(C 4-9 alkyl), —N(R 12 )(C 3-10 cycloalkyl), —N(R 12 )(4-20 membered heterocyclyl), —N(R 12 )(aryl), —N(R 12 )(heteroaryl), —N(R 12 )C(O)O(C 4-9 alkyl), —N(R 12 )C(O)O(C 3-10 cycloalkyl), —N(R 12 )C(O)O(4-20 membered heterocyclyl), —N(R 12 )C(O)O(aryl), —N(R 12 )C(O)O(heteroaryl), —C(O)N(R 12 )(C 5-9 alkyl), —C(O)N(R 12 )(C 7-10 cycloalkyl), —C(O)N(R 12 )(4-20 membered heterocyclyl), —C(O)N(R 12 )(aryl), —C(O)N(R 12 )(heteroaryl), —C(O)N(R 9 )(R 9 ), —C(O)O—R 12 , —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O) 2 R 12 , —S(O)(NH)R 12 , or —S(O) 2 N(R 12 )(R 12 );

wherein said C 4-6 cycloalkyl is also optionally substituted with Z 1 ;

wherein said C 1-4 alkyl is optionally substituted with oxo, halo, —NO 2 , —CN, —N 3 , C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 16 , —O(C 4-9 alkyl), —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein each said C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, —O(C 4-9 alkyl), —O(C 3-10 cycloalkyl), —O(heterocyclyl), —O(aryl), —O(heteroaryl), —N(R 12 )C(O)(C 5-9 alkyl), —N(R 12 )C(O)(C 3-10 cycloalkyl), —N(R 12 )C(O)(heterocyclyl), —N(R 12 )C(O)(aryl), —N(R 12 )C(O)(heteroaryl), —N(R 12 )(C 4-9 alkyl), —N(R 12 )(C 3-10 cycloalkyl), —N(R 12 )(heterocyclyl), —N(R 12 )(aryl), —N(R 12 )(heteroaryl), —N(R 12 )C(O)O(C 4-9 alkyl), —N(R 12 )C(O)O(C 3-10 cycloalkyl), —N(R 12 )C(O)O(heterocyclyl), —N(R 12 )C(O)O(aryl), —N(R 12 )C(O)O(heteroaryl), —C(O)N(R 12 )(C 5-9 alkyl), —C(O)N(R 12 )(C 7-10 cycloalkyl), —C(O)N(R 12 )(heterocyclyl), —C(O)N(R 12 )(aryl), —C(O)N(R 12 )(heteroaryl), aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1a .

51. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 4-6 cycloalkyl substituted with one or more substituents selected from C 1-4 hydroxyalkyl, C 1-3 alkoxy, —(CH 2 ) 1-3 O(C 1-3 alkyl), —C(O)NH(C 1-4 alkyl), —C(O)NH(C 3-6 cycloalkyl), —N(C 1-3 alkyl) 2 , —NHC(O)O(C 1-3 alkyl), —NHC(O)(C 1-4 hydroxyalkyl);

wherein said C 4-6 cycloalkyl is optionally substituted with Z 1 ;

wherein said —C(O)NH(C 3-6 cycloalkyl) is substituted with Z 1a ;

wherein said C 1-4 hydroxyalkyl or —NHC(O)(C 1-4 hydroxyalkyl) is substituted with oxo, halo, —NO 2 , —CN, —N 3 , C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 ) S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 1-3 alkoxy, —(CH 2 ) 1-3 O(C 1-3 alkyl), —N(C 1-3 alkyl) 2 , —NHC(O)O(C 1-3 alkyl) is substituted with oxo, halo, —NO 2 , —CN, —N 3 , C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said —C(O)NH(C 1-4 alkyl) is substituted with oxo, halo, —NO 2 , —CN, —N 3 , C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein each said C 3-9 alkyl, C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1b .

52. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 4-6 cycloalkyl substituted with one or more —NHC(O)(C 1-3 alkyl);

wherein at least one —NHC(O)(C 1-3 alkyl) is substituted with one or more oxo, halo, —NO 2 , —CN, —N 3 , C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 4-6 cycloalkyl is optionally substituted with Z 1 ; and

wherein said C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1a .

53. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is C 4-6 cycloalkyl substituted with three or more substituents selected from —OH, C 1-4 hydroxyalkyl, C 1-3 alkoxy, —(CH 2 ) 1-3 O(C 1-3 alkyl), —C(O)NH(C 1-4 alkyl), —C(O)NH(C 3-6 cycloalkyl), —N(C 1-3 alkyl) 2 , —NHC(O)(C 1-3 alkyl), —NHC(O)O(C 1-3 alkyl), or —NHC(O)(C 1-4 hydroxyalkyl);

wherein said C 4-6 cycloalkyl is optionally substituted with Z 1 .

54. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is s 5-10 membered heteroaryl optionally substituted with Z 1 .

55. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is oxazolyl, isoxazolyl, thiadiazole, thiazole, oxadiazole, isothiazolyl, tetrazolyl, thiophenyl, furanyl, or a 6-10 membered heteroaryl; any of which is optionally substituted with Z 1 .

56. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is 4-7 membered monocyclic heterocyclyl optionally substituted with Z 1 .

57. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is azetidinyl, oxetanyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, 4-7 membereded sultam, 4-7 membered cyclic carbamate, 4-7 membered cyclic carbonate, or 4-7 membered cyclic sulfide; any of which is optionally substituted with Z 1 .

58. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl;

wherein said tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl is substituted with one or more substituents selected from oxo, halo, —CN, C 2-4 alkyl, C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O) 2 (C 4-9 alkyl), —S(O) 2 (C 3-10 cycloalkyl), —S(O) 2 (4-20 membered heterocyclyl), —S(O) 2 (aryl), —S(O) 2 (heteroaryl), —S(O)(NH)R 12 , or —S(O) 2 N(R 12 )(R 12 );

wherein said tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl, pyrrolyl, pyrazolyl, imidazolyl, or triazolyl is optionally substituted with Z 1a ;

wherein said C 2-4 alkyl is optionally substituted with halo, —NO 2 , —CN, —N 3 , C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein each said C 3-9 alkyl, C 5-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —S(O) 2 (C 4-9 alkyl), —S(O) 2 (C 3-10 cycloalkyl), —S(O) 2 (heterocyclyl), —S(O) 2 (aryl), or —S(O) 2 (heteroaryl) is optionally substituted with Z 1a .

59. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl;

wherein said tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl is substituted with one or more C 1 alkyl;

wherein said tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl, pyrrolyl, pyrazolyl, imidazolyl, or triazolyl is optionally substituted with Z 1 ;

wherein said C 1 alkyl is optionally substituted with oxo, halo, —NO 2 , —CN, —N 3 , C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 9 )(R 9 ), —C(O)N(R 12 )(C 4-9 alkyl), —C(O)N(R 12 )(C 3-10 cycloalkyl), —C(O)N(R 12 )(4-20 membered heterocyclyl), —C(O)N(R 12 )(aryl), —C(O)N(R 12 )(heteroaryl), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —C(O)N(R 12 )(C 3-10 cycloalkyl), —C(O)N(R 12 )(heterocyclyl), —C(O)N(R 12 )(aryl), —C(O)N(R 12 )(heteroaryl) is optionally substituted with Z 1a .

60. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl; any of which is optionally substituted with Z 1 ;

wherein said tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl is substituted with one or more S(O) 2 (C 1-3 alkyl);

wherein said S(O) 2 (C 1-3 alkyl) is substituted with oxo, halo, —NO 2 , —CN, —N 3 , C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1b .

61. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl; any of which is optionally substituted with Z 1 ;

wherein said tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl is substituted with one or more C 1-4 hydroxyalkyl;

wherein said C 1-4 hydroxyalkyl is substituted with oxo, halo, —NO 2 , —CN, —N 3 , C 4-9 alkyl,C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1b .

62. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl; any of which is optionally substituted with Z 1 ;

wherein said tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl is substituted with one or more —CH 2 C(O)NH(C 1-6 alkyl);

wherein said —CH 2 C(O)NH(C 1-6 alkyl) is substituted with oxo, —Cl, —NO 2 , —CN, —N 3 , C 6-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said —CH 2 C(O)NH(C 1-6 alkyl) is optionally substituted with Z 1a ; and

wherein said C 6-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1b .

63. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl, pyrrolyl, pyrazolyl, imidazolyl, or triazolyl;

wherein said tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl, pyrrolyl, pyrazolyl, imidazolyl, or triazolyl is substituted with one or more —CH 2 C(O)NH(C 4-6 alkyl); and

wherein said tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, piperazinyl pyrrolyl, pyrazolyl, imidazolyl, or triazolyl is optionally substituted with Z 1 .

64. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is C 6-10 aryl optionally substituted with Z 1 .

65. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 2 is 6-12 membered bicyclic heterocyclyl optionally substituted with Z 1 ;

wherein when said 6-12 membered bicyclic heterocyclyl is 1-oxa-7-azaspiro[3.5]nonanyl, then said 1-oxa-7-azaspiro[3.5]nonanyl is substituted with one or more Z 1 .

66. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 2 is —N(R 12 )(R 12 ) —S(O) 2 R 12 ) —S(O) 2 N(R 12 )(R 12 ); or —H.

67. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 3 is selected from H, halo, —NO 2 , —CN, —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )C(O)—N(R 12 )(R 12 ), —S(O) 2 R 12 ), —SR 12 and —S(O) 2 N(R 12 )(R 12 ).

68. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 3 is selected from —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 9 )(R 9 ), —NH(R 9 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )C(O)—N(R 12 )(R 12 ), —S(O) 2 (R 12 ), —S—R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein when said —N(H)(R 9 ) is NH(C 1-3 alkyl), —N(H)(R 9 ) is NH(C 1-4 hydroxyalkyl), or —O—R 12 is —O(C 1-3 alkyl), then said NH(C 1-3 alkyl), NH(C 1-4 hydroxyalkyl), or —O(C 1-3 alkyl) is further substituted with one or more oxo, halo, —NO 2 , —CN, —N 3 , C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1a .

69. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 3 is selected from —O(C 4 alkyl) or —N(H)(C 4 alkyl); wherein said —O(C 4 alkyl) is optionally substituted with Z 1a ; wherein said —N(H)(C 4 alkyl) is optionally substituted with oxo, halo —NO 2 , —CN, —N 3 , C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1a .

70. The compound of claims 1 claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is C 1-9 alkyl optionally substituted with Z 1 .

71. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 3 is C 1-2 alkyl optionally substituted with F and further substituted with one or more oxo, —Cl, —NO 2 , —N 3 , —CN, C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1a .

72. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is C 3 alkyl substituted with one or more Z 1 .

73. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is C 4-9 alkyl optionally substituted with Z 1 .

74. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is C 2-9 alkynyl optionally substituted with Z 1 .

75. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is C 2-9 alkenyl optionally substituted with Z 1 .

76. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is a 5-10 membered heteroaryl optionally substituted with Z 1 .

77. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 3 is a 5-10 membered heteroaryl optionally substituted with Z 1 ;

wherein if said 5-10 membered heteroaryl is pyridinyl, then said pyridinyl is further substituted with one or more Z 1 .

78. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is C 6-10 aryl optionally substituted with Z 1 .

79. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 3 is C 6-10 aryl optionally substituted with Z 1 ;

wherein when said C6-10 aryl is cyanophenyl then said cyanophenyl is further substituted with one or more oxo, halo —NO 2 , —N 3 , C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl is optionally substituted with Z 1a .

80. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is a 4-12 membered heterocyclyl optionally substituted with Z 1 .

81. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 3 is a 4-12 membered heterocyclyl optionally substituted with Z 1 ;

wherein when said 4-12 membered heterocyclyl is hydroxypyrrolidinyl then said hydroxypyrrolidinyl is further substituted with one or more oxo, halo, —CN, —CN, —NO 2 , —N 3 , C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or 4-20 membered heterocyclyl is optionally substituted with Z 1a .

82. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is C 3-10 cycloalkyl optionally substituted with Z 1 .

83. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is C 3-6 cycloalkyl substituted with one or more Z 1 .

84. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is C 7-10 cycloalkyl optionally substituted with Z 1 .

85. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is H, halo, —NO 2 , —CN, —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )C(O)—N(R 12 )(R 12 ), —S(O) 2 R 12 ), —SR 12 or —S(O) 2 N(R 12 )(R 12 ).

86. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 4 is —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 9 )(R 9 ), —NH(R 9 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )C(O)—N(R 12 )(R 12 ), —S(O) 2 (R 12 ), —S—R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein when said —N(H)(R 9 ) is NH(C 1-3 alkyl), —N(H)(R 9 ) is NH(C 1-4 hydroxyalkyl), or —O—R 12 is —O(C 1-3 alkyl), then said NH(C 1-3 alkyl), NH(C 1-4 hydroxyalkyl), or —O(C 1-3 alkyl) is further substituted with one or more oxo, halo, —NO 2 , —CN, —N 3 , C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 4-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1a .

87. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 4 is selected from —O(C 4 alkyl) or —N(H)(C 4 alkyl); wherein said —O(C 4 alkyl) is optionally substituted with Z 1a ;

wherein said —N(H)(C 4 alkyl) is optionally substituted with oxo, halo, —NO 2 , —CN, —N 3 , C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(V), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl is optionally substituted with Z 1a .

88. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is C 1-9 alkyl optionally substituted with Z 1 .

89. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 4 is C 1-2 alkyl optionally substituted with F and further substituted with one or more oxo, —Cl, —NO 2 , —N 3 , —CN, C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with Z 1a .

90. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is C 3 alkyl substituted with one or more Z 1 .

91. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is C 4-9 alkyl optionally substituted with Z 1 .

92. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is C 2-9 alkynyl optionally substituted with Z 1 .

93. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is C 2-9 alkenyl optionally substituted with Z 1 .

94. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is a 5-10 membered heteroaryl optionally substituted with Z 1 .

95. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 4 is a 5-10 membered heteroaryl optionally substituted with Z 1 ;

wherein when said 5-10 membered heteroaryl is pyridinyl then said pyridinyl is further substituted with one or more Z 1 .

96. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is C 6-10 aryl optionally substituted with Z 1 .

97. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 4 is C 6-10 aryl optionally substituted with Z 1 ;

wherein when said C 6-10 aryl is cyanophenyl then said cyanophenyl is further substituted with one or more oxo, halo, —NO 2 , —N 3 , C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —NR 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —NR 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —NR 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein said C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl is optionally substituted with Z 1a .

98. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is a 4-12 membered heterocyclyl optionally substituted with Z 1 .

99. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

R 4 is a 4-12 membered heterocyclyl optionally substituted with Z 1 ; wherein when said 4-12 membered heterocyclyl is hydroxypyrrolidinyl then said hydroxypyrrolidinyl is further substituted with one or more oxo, halo, —CN, —NO 2 , —N 3 , C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 9 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein said C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl is optionally substituted with Z 1a .

100. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is C 3-10 cycloalkyl optionally substituted with Z 1 .

101. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is C 3-6 cycloalkyl substituted with one or more Z 1 .

102. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is C 7-10 cycloalkyl optionally substituted with Z 1 .

103. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein at least one of R 5 , R 6 or R 7 is independently selected from H, halo, —NO 2 , —CN, —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 9 )(R 9 ), NH(R 9 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , or —N(R 12 )S(O) 2 (R 12 ).

104. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein at least one of R 5 , R 6 or R 7 is independently selected from —NO 2 , —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 9 )(R 9 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , or —N(R 12 )S(O) 2 (R 12 ).

105. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein at least one of R 5 , R 6 or R 7 is independently C 1-5 alkyl optionally substituted with Z 1 .

106. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein at least one of R 5 , R 6 or R 7 is independently C 1-2 alkyl optionally substituted with F and substituted with one or more oxo, —Cl, —NO 2 , —N 3 , —CN, C 3-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 2 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); wherein any alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1a .

107. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein at least one of R 5 , R 6 or R 7 is independently C 3 alkyl substituted with one or more Z 1 .

108. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein at least one of R 5 , R 6 or R 7 is independently C 4-5 alkyl optionally substituted with Z 1 .

109. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein at least one of R 5 , R 6 or R 7 is independently cyclopropyl, oxetanyl, or azetidinyl optionally substituted with Z 1 .

110. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein at least one of R 5 , R 6 or R 7 is independently cyclopropyl, oxetanyl, or azetidinyl; wherein said cyclopropyl is substituted with one or more Z 1 ; wherein said oxetanyl or azetidinyl is optionally substituted with Z 1 .

111. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein no more than two of R 3 , R 4 , R 5 , R 6 or R 7 are H.

112. The compound of any of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 3 is H or F.

113. The compound of any of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 4 is H, F, —CN or Cl.

114. The compound of any of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 5 is H or F.

115. The compound of any of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 6 is H or F.

116. The compound of any of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 7 is H or F.

117. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein:

Z 1 is selected H, halo, —CN, C 1-9 alkyl, C 3-15 cycloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )S(O) 2 (R 12 ), —OC(O)—N(R 12 )(R 12 ), —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 ); and

wherein any alkyl, cycloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1a .

118. A pharmaceutical composition comprising an effective amount of a compound of claim 1 , together with a pharmaceutically acceptable carrier, and optionally a diluent.

119. A method of treating an inflammation related disease or disorder in a patient in need thereof, comprising administering to said patient a compound of claim 1 , or a pharmaceutical composition containing a compound of claim 1 , and wherein the inflammation related disease or disorder is selected from the group consisting of: rheumatoid arthritis (RA), inflammatory bowel disease (IBD), gout, Lyme arthritis, systemic lupus erythematosus (SLE), Sjogren's syndrome, viral myocarditis. Aicardi-Goutieres syndrome, Familial chilblain lupus, and Retinal vasculopathy with cerebral leukodystrophy.

120. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is 5-10 membered heteroaryl optionally substituted with Z 1 , wherein when said 5-10 membered heteroaryl is furanyl, pyranyl, pyrraolyl, imidazolyl, pyrazolyl, triazoyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, thiaphenyl, oxazoyl, thiazoyl, said 5-10 membered heteroaryl is optionally substituted with a 5-12 membered bicyclic ring or a 5-12 membered hetero bicyclic ring, wherein the bicyclic ring and the hetero bicyclic ring may be fused, spiro or bridged.

121. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, wherein R 1 is 5-12 membered bicyclic ring optionally substituted with Z 1 .

122. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, R 1 is 5-12 membered bicyclic ring optionally substituted with C 1-3 alkyl, C 2-6 alkenyl, C 2-6 alkynl, 3-6 membered cyclo alkyl, 3-6 membered heterocyclyl, 5-6 membered aryl, or 5-6 membered heteroaryl, where the C 1-3 alkyl, C 2-6 alkenyl, C 2-6 alkynl, 3-6 membered cyclo alkyl, 3-6 membered heterocyclyl, 5-6 membered aryl, or 5-6 membered heteroaryl groups can further be substituted with one or more Z 1a groups.

123. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, R 1 is 5-12 membered bicyclic heterocyclyl optionally substituted with Z 1 .

124. The compound of claim 1 , or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof, R 1 is 5-12 membered bicyclic heterocyclyl optionally substituted with C 1-3 alkyl, C 2-6 alkenyl, C 2-6 alkynl, 3-6 membered cyclo alkyl, 3-6 membered heterocyclyl, 5-6 membered aryl, or 5-6 membered heteroaryl, where the C 1-3 alkyl, C 2-6 alkenyl, C 2-6 alkynl, 3-6 membered cyclo alkyl, 3-6 membered heterocyclyl, 5-6 membered aryl, or 5-6 membered heteroaryl groups can further be substituted with one or more Z 1a groups.

125. A compound of Formula (I)

wherein:

R 1 and R 2 are each independently selected from:

h) C 1-10 alkyl optionally substituted with Z 1 ;

i) C 3-10 cycloalkyl optionally substituted with Z 1 ;

j) 5-10 membered heteroaryl optionally substituted with Z 1 ;

k) C 6-10 aryl optionally substituted with Z 1 ;

l) 4-7 membered monocyclic heterocyclyl optionally substituted with Z 1 ;

m) 6-12 membered bicyclic heterocyclyl optionally substituted with Z 1 ; or

n) —N(R 12 )(R 12 ), —S(O) 2 R 12 , S(O) 2 N(R 12 )(R 12 ), or —H;

wherein when R 1 or R 2 is C 1-10 alkyl, C 3-10 cycloalkyl, 5-10 membered heteroaryl, C 6-10 aryl, 4-7 membered monocyclic heterocyclyl, 6-12 membered bicyclic heterocyclyl, two Z 1 groups either attached to the same atom on R 1 or R 2 , or two Z 1 groups attached to adjacent atoms on R 1 or R 2 , append together to form a 3-6 membered cycloalkyl or 3-6 membered heterocyclyl;

R 3 and R 4 are each independently selected from:

i) H, halo, —NO 2 , —CN, —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N( R 12 )(R 12 ), —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )C(O)—N(R 12 )(R 12 ), —S(O) 2 R 12 or —S(O) 2 N(R 12 )( R 12 );

j) C 1-9 alkyl optionally substituted with Z 1 ;

k) C 2-9 alkynyl optionally substituted with Z 1 ;

l) C 2-9 alkenyl optionally substituted with Z 1 ;

m) 5-10 membered heteroaryl optionally substituted with Z 1 ;

n) C 6-10 aryl optionally substituted with Z 1 ;

o) 4-12 membered heterocyclyl optionally substituted with Z 1 ; or

p) C 3-10 cycloalkyl optionally substituted with Z 1 ;

R 5 , R 6 and R 7 are each independently selected from:

d) H, halo, —NO 2 , —CN, —O—R 12 , —C(O)—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 )—C(O)—

R 12 , —N(R 12 )C(O)O—R 12 , or —N(R 12 )S(O) 2 (R 12 ;

e) C 1-5 alkyl optionally substituted with Z 1 ; or

f) Cyclopropyl, oxetanyl or azetidinyl optionally substituted with Z 1 ;

Z 1 is independently oxo, halo, —NO 2 , —N 3 , —CN, C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O—R 12 , —C(O)—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)—R 12 , —N(R 12 )C(O)O—R 12 , —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1a ;

each Z 1a is independently oxo, halo, —NO 2 , —CN, —N 3 , C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —O—R 12 , —C(O)R 12 , —C(O)O—R 12 , —C(O)N(R 12 )(R 12 ), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )—C(O)R 12 , —N(R 12 )C(O)O(R 12 ), —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —N(R 12 )S(O) 2 —N(R 12 )(R 12 ), —N(R 12 )S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z ib ;

each R 12 is independently H, C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl or 4-20 membered heterocyclyl, wherein the C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, aryl, heteroaryl or heterocyclyl can further optionally be substituted with one or more Z 1a group;

each Z 1b is independently oxo, hydroxy, halo, —NO 2 , —N 3 , —CN, C 1-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, 4-20 membered heterocyclyl, —O(C 1-9 alkyl), —O(C 2-6 alkenyl), —O(C 2-6 alkynyl), —O(C 3-15 cycloalkyl), —O(C 1-8 haloalkyl), —O(aryl), —O(heteroaryl), —O(4-20 membered heterocyclyl), —NH 2 , —NH(C 1-9 alkyl), —NH(C 2-6 alkenyl), —NH(C 2-6 alkynyl), —NH(C 3-15 cycloalkyl), —NH(C 1-8 haloalkyl), —NH(aryl), —NH(heteroaryl), —NH(4-20 membered heterocyclyl), —N(C 1-9 alkyl) 2 , —N(C 3-15 cycloalkyl) 2 , —N(C 2-6 alkenyl) 2 , —N(C 2-6 alkynyl) 2 , —N(C 3-15 cycloalkyl) 2 , —N(C 1-8 haloalkyl) 2 , —N(aryl) 2 , —N(heteroaryl) 2 , —N(4-20 membered heterocyclyl) 2 , —N(C 1-9 alkyl)(C 3-15 cycloalkyl), —N(C 1-9 alkyl)(C 2-6 alkenyl), —N(C 1-9 alkyl)(C 2-6 alkynyl), —N(C 1-9 alkyl)(C 3-15 cycloalkyl), —N(C 1-9 alkyl)(C 1-8 haloalkyl), —N(C 1-9 alkyl)(aryl), —N(C 1-9 alkyl)(heteroaryl), —N(C 1-9 alkyl)(4-20 membered heterocyclyl), —C(O)(C 1-9 alkyl), —C(O)(C 2-6 alkenyl), —C(O)(C 2-6 alkynyl), —C(O)(C 3-15 cycloalkyl), —C(O)(C 1-8 haloalkyl), —C(O)(aryl), —C(O)(heteroaryl), —C(O)(4-20 membered heterocyclyl), —C(O)O(C 1-9 alkyl), —C(O)O(C 2-6 alkenyl), —C(O)O(C 2-6 alkynyl), —C(O)O(C 3-15 cycloalkyl), —C(O)O(C 1-8 haloalkyl), —C(O)O(aryl), —C(O)O(heteroaryl), —C(O)O(4-20 membered heterocyclyl), —C(O)NH 2 , —C(O)NH(C 1-9 alkyl), —C(O)NH(C 2-6 alkenyl), —C(O)NH(C 2-6 alkynyl), —C(O)NH(C 3-15 cycloalkyl), —C(O)NH(C 1-8 haloalkyl), —C(O)NH(aryl), —C(O)NH(heteroaryl), —C(O)NH(4-20 membered heterocyclyl), —C(O)N(C 1-9 alkyl) 2 , —C(O)N(C 3-15 cycloalkyl) 2 , —C(O)N(C 2-6 alkenyl) 2 , —C(O)N(C 2-6 alkynyl) 2 , —C(O)N(C 3-15 cycloalkyl) 2 , —C(O)N(C 1-8 haloalkyl) 2 , —C(O)N(aryl) 2 , —C(O)N(heteroaryl) 2 , —C(O)N(4-20 membered heterocyclyl) 2 , —NHC(O)(C 1-9 alkyl), —NHC(O)(C 2-6 alkenyl), —NHC(O)(C 2-6 alkynyl), —NHC(O)(C 3-15 cycloalkyl), —NHC(O)(C 1-8 haloalkyl), —NHC(O)(aryl), —NHC(O)(heteroaryl), —NHC(O)(4-20 membered heterocyclyl), —NHC(O)O(C 1-9 alkyl), —NHC(O)O(C 2-6 alkenyl), —NHC(O)O(C 2-6 alkynyl), —NHC(O)O(C 3-15 cycloalkyl), —NHC(O)O(C 1-8 haloalkyl), —NHC(O)O(aryl), —NHC(O)O(heteroaryl), —NHC(O)O(4-20 membered heterocyclyl), —NHC(O)NH(C 1-9 alkyl), —NHC(O)NH(C 2-6 alkenyl), —NHC(O)NH(C 2-6 alkynyl), —NHC(O)NH(C 3-15 cycloalkyl), —NHC(O)NH(C 1-8 haloalkyl), —NHC(O)NH(aryl), —NHC(O)NH(heteroaryl), —NHC(O)NH(4-20 membered heterocyclyl), —SH, —S(C 1-9 alkyl), —S(C 2-6 alkenyl), —S(C 2-6 alkynyl), —S(C 3-15 cycloalkyl), —S(C 1-8 haloalkyl), —S(aryl), —S(heteroaryl), —S(4-20 membered heterocyclyl), —NHS(O)(C 1-9 alkyl), —N(C 1-9 alkyl)(S(O)(C 1-9 alkyl), —S(O)N(C 1-9 alkyl) 2 , —S(O)(C 1-9 alkyl), —S(O)(NH)(C 1-9 alkyl), —S(O)(C 2-6 alkenyl), —S(O)(C 2-6 alkynyl), —S(O)(C 3-15 cycloalkyl), —S(O)(C 1-8 haloalkyl), —S(O)(aryl), —S(O)(heteroaryl), —S(O)(4-20 membered heterocyclyl), —S(O) 2 (C 1-9 alkyl), —S(O) 2 (C 2-6 alkenyl), —S(O) 2 (C 2-6 alkynyl), —S(O) 2 (C 3-15 cycloalkyl), —S(O) 2 (C 1-8 haloalkyl), —S(O) 2 (aryl), —S(O) 2 (heteroaryl), —S(O) 2 (heterocyclyl), —S(O) 2 NH(C 1-9 alkyl), or —S(O) 2 N(C 1-9 alkyl) 2 ;

wherein any alkyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with one or more halo, C 1-9 alkyl, C 1-8 haloalkyl, —OH, —NH 2 , —NH(C 1-9 alkyl), —NH(C 3-15 cycloalkyl), —NH(C 1-8 haloalkyl), —NH(aryl), —NH(heteroaryl), —NH(heterocyclyl), —N(C 1-9 alkyl) 2 , —N(C 3-15 cycloalkyl) 2 , —NHC(O)(C 3-15 cycloalkyl), —NHC(O)(C 1-8 haloalkyl), —NHC(O)(aryl), —NHC(O)(heteroaryl), —NHC(O)(heterocyclyl), —NHC(O)O(C 1-9 alkyl), —NHC(O)O(C 2-6 alkynyl), —NHC(O)O(C 3-15 cycloalkyl), —NHC(O)O(C 1-8 haloalkyl), —NHC(O)O(aryl), —NHC(O)O(heteroaryl), —NHC(O)O(heterocyclyl), —NHC(O)NH(C 1-9 alkyl), —S(O)(NH)(C 1-9 alkyl), S(O) 2 (C 1-9 alkyl), —S(O) 2 (C 3-15 cycloalkyl), —S(O) 2 (C 1-8 haloalkyl), —S(O) 2 (aryl), —S(O) 2 (heteroaryl), —S(O) 2 (heterocyclyl), —S(O) 2 NH(C 1-9 alkyl), —S(O) 2 N(C 1-9 alkyl) 2 , —O(C 3-15 cycloalkyl), —O(C 1-8 haloalkyl), —O(aryl), —O(heteroaryl), —O(heterocyclyl), or —O(C 1-9 alkyl); and

with the proviso that when R 1 is C 3 alkyl, R 2 is C 5 alkyl substituted with F and hydroxyl, R 3 , R 5 , R 6, R 7 are H, and R 4 is CN, then R 1 is substituted with oxo, halo, —NO 2 , —N 3 , —CN, C 2-9 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-15 cycloalkyl, C 1-8 haloalkyl, aryl, heteroaryl, heterocyclyl, —O—R 12 , —C(O)O—R 12 , —C(O)—N(R 12 )(R 12), —N(R 12 )(R 12 ), —N(R 12 ) 2 (R 12 ) + , —N(R 12 )C(O)O—R 12—, —N(R 12 )C(O)N(R 12 )(R 12 ), —N(R 12 )S(O) 2 (R 12 ), —NR 12 S(O) 2 N(R 12 )(R 12 ), —NR 12 S(O) 2 O(R 12 ), —OC(O)R 12 , —OC(O)OR 12 , —OC(O)—N(R 12 )(R 12 ), —Si(R 12 ) 3 , —S—R 12 , —S(O)R 12 , —S(O)(NH)R 12 , —S(O) 2 R 12 or —S(O) 2 N(R 12 )(R 12 );

wherein any alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, aryl, heteroaryl or heterocyclyl is optionally substituted with Z 1a ;

or a pharmaceutically acceptable salt, stereoisomer, mixture of stereoisomers, or deuterated analog thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2018
From: BACON, ELIZABETH M.; BRIZGYS, GEDIMINAS; CHIN, ELBERT; CHOU, CHIEN-HUNG; COTTELL, JEROMY J.; LINK, JOHN O.; TAYLOR, JAMES G.; TSE, WINSTON C.; WRIGHT, NATHAN E.; YANG, ZHENG-YU; ZHANG, JENNIFER R.; ZIPFEL, SHEILA M.
To: GILEAD SCIENCES, INC.
Reel/Frame 045123/0523 →
Continuity (2)
Provisional Application 62460013 · Feb 16, 2017
Related Publication 20180230157A1 · Aug 16, 2018
Cited By (3)
US 12,415,808 US 12,528,814 US 12,570,662