IP Library › Granted Patent US 9,896,432
Granted Patent B2
US 9,896,432 · App. 15/647,758 · Granted Feb 20, 2018

Somatostatin modulators and uses thereof

Inventors: Jian Zhao (San Diego, CA); Sangdon Han (San Diego, CA); Sun Hee Kim (San Diego, CA); Shimiao Wang (San Diego, CA); Yunfei Zhu (San Diego, CA)
Assignee: CRINETICS PHARMACEUTICALS, INC.
C07D401/04C07D401/14C07D405/14C07D413/14C07D471/04C07D498/04
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Quick Facts
Patent No.
US 9,896,432
App. No.
15/647,758
Granted
Feb 20, 2018
Kind
B2
Abstract

Described herein are compounds that are somatostatin modulators, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders that would benefit from modulation of somatostatin activity.

Claims (94)

1. A compound that has the structure of Formula (AIIb), or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof:

wherein:

each R a and R b is independently hydrogen, halogen, unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted or substituted C 1 -C 6 fluoroalkyl, unsubstituted or substituted C 1 -C 6 heteroalkyl, unsubstituted or substituted monocyclic carbocycle, unsubstituted or substituted monocyclic heterocycle, —CN, —OH, —OR 14 , —CO 2 R 15 , —CH 2 CO 2 R 15 , —C(═O)N(R 15 ) 2 , —CH 2 C(═O)N(R 15 ) 2 , —N(R 15 ) 2 , —CH 2 N(R 15 ) 2 , —CH(CF 3 )N(R 15 ) 2 , —NR 15 C(═O)R 14 , —CH 2 NR 15 C(═O)R 14 , —SR 14 , —S(═O)R 14 , —SO 2 R 14 , —SO 2 N(R 15 ) 2 or —C(═NOR 15 )R 15 ;

m is 1 or 2; n is 0, 1 or 2;

or if one R a and one R b are on adjacent atoms then the adjacent R a and R b groups are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted 5- or 6-membered monocyclic carbocycle or an unsubstituted or substituted 5- or 6-membered monocyclic heterocycle;

R B is an unsubstituted or substituted ring B that is an unsubstituted or substituted phenyl or an unsubstituted or substituted pyridinyl, wherein if the ring B is substituted then the ring B is substituted with p R c and q R d ;

each R c and R d is independently hydrogen, halogen, unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted or substituted C 1 -C 6 fluoroalkyl, unsubstituted or substituted monocyclic carbocycle, unsubstituted or substituted monocyclic heterocycle, —CN, —OH, —OR 14 , —C(═O)R 15 , —OC═O)R 15 , —CO 2 R 15 , —CH 2 CO 2 R 15 , —C(═O)N(R 15 ) 2 , —OC(═O)N(R 15 ) 2 , —NR 15 C(═O)N(R 15 ) 2 , —NR 15 C(═O)OR 14 , —NR 15 C(═O)NR 15 OR 14 , —C(═O)NR 15 OR 15 , —CH 2 C(═O)N(R 15 ) 2 , —N(R 15 ) 2 , —CH 2 N(R 15 ) 2 , —CH(CF 3 )N(R 15 ) 2 , —NR 15 C(═O)R 14 , —CH 2 NR 15 C(═O)R 14 , —SR 14 , —S(═O)R 14 , —SO 2 R 14 , —SO 2 N(R 15 ) 2 , —C(═NOR 15 )R 15 , —N(R 15 )SO 2 R 14 , —C(═O)NR 15 S(═O) 2 R 14 , —S(═O) 2 NR 15 C(═O)R 14 , —C(═NR 15 )N(R 15 ) 2 , —NR 15 C(═NR 15 )N(R 15 ) 2 , —NR 15 C(═CR 14 R 15 )N(R 15 ) 2 , —C(═O)NR 15 C(═NR 15 )N(R 15 ) 2 or, —C(═O)NR 15 C(═CR 14 R 15 )N(R 15 ) 2 ;

p is 1 or 2; q is 0, 1 or 2;

or if one R c and one R d are on adjacent atoms of ring B then the adjacent R c and R d groups are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted 5- or 6-membered monocyclic carbocycle or an unsubstituted or substituted 5- or 6-membered monocyclic heterocycle;

R e is hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, —CN, OH, or —OR 14 ;

each R f is independently hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, —CN, —OH, or —OR 14 ;

R 1 and R 2 are independently hydrogen, unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted or substituted C 1 -C 6 heteroalkyl, unsubstituted or substituted C 1 -C 6 fluoroalkyl, unsubstituted or substituted C 3 -C 6 cycloalkyl or substituted or unsubstituted C 2 -C 6 heterocycloalkyl;

or R 1 and R 2 are taken together with the nitrogen atom to which they are attached to form ring C that is an unsubstituted or substituted N-containing C 2 -C 8 heterocycloalkyl;

R 5 is selected from the group consisting of hydrogen, halogen, —OH, —OR 14 , —SR 14 , —S(═O)R 14 , —S(═O) 2 R 14 , —N(R 15 ) 2 , —CN, —C(═O)OR 15 , —C(═O)N(R 15 ) 2 , unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted or substituted C 1 -C 6 heteroalkyl, and unsubstituted or substituted C 1 -C 6 fluoroalkyl;

or R 2 and R 5 are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted 4-7 membered saturated N-containing heterocyclic ring;

each R 14 is independently selected from unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted or substituted C 1 -C 6 heteroalkyl, unsubstituted or substituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl;

each R 15 is independently selected from hydrogen, unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted or substituted C 1 -C 6 heteroalkyl, unsubstituted or substituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl;

or two R 15 on the same N atom are taken together with the N atom to which they are attached to form an unsubstituted or substituted N-containing heterocycle;

wherein each substituted alkyl, substituted fluoroalkyl, substituted heteroalkyl, substituted carbocycle, and substituted heterocycle is substituted with one or more R s groups independently selected from the group consisting of halogen, C 1 -C 6 alkyl, monocyclic carbocycle, monocyclic heterocycle, —CN, —OR 16 , —CO 2 R 16 , —C(═O)N(R 16 ) 2 , —N(R 16 ) 2 , —NR 16 C(═O)R 17 , —SR 16 , —S(═O)R 17 , —SO 2 R 17 , or —SO 2 N(R 16 ) 2 ;

each R 16 is independently selected from hydrogen, C 1 -C 6 alkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 heterocycloalkyl, phenyl, benzyl, 5-membered heteroaryl and 6-membered heteroaryl; or two R 16 groups are taken together with the N atom to which they are attached to form a N-containing heterocycle;

each R 17 is independently selected from C 1 -C 6 alkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 heterocycloalkyl, phenyl, benzyl, 5-membered heteroaryl and 6-membered heteroaryl.

2. The compound of claim 1 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

R e is hydrogen, F, Cl, Br, —CH 3 , —CH 2 CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , —OCH 2 CH 3 , or —OCF 3 ;

each R f is independently hydrogen, F, Cl, Br, —CH 3 , —CH 2 CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , —OCH 2 CH 3 , or —OCF 3 .

3. The compound of claim 2 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

each R a is independently hydrogen, halogen, unsubstituted or substituted C 1 -C 4 alkyl, unsubstituted or substituted C 1 -C 4 fluoroalkyl, unsubstituted or substituted C 1 -C 4 heteroalkyl, —CN, —OH, —OR 14 , —CO 2 R 15 , —CH 2 CO 2 R 15 , —C(═O)N(R 15 ) 2 , —CH 2 C(═O)N(R 15 ) 2 , —N(R 15 ) 2 , —CH 2 N(R 15 ) 2 , —CH(CF 3 )N(R 15 ) 2 , —NR 15 C(═O)R 14 , —CH 2 NR 15 C(═O)R 14 , —SR 14 , —S(═O)R 14 , —SO 2 R 14 , —SO 2 N(R 15 ) 2 or; and

each R b is independently hydrogen, halogen, unsubstituted or substituted C 1 -C 4 alkyl, unsubstituted or substituted C 1 -C 4 fluoroalkyl, unsubstituted or substituted C 1 -C 4 heteroalkyl, —CN, —OH, or —O-(unsubstituted or substituted C 1 -C 4 alkyl).

4. The compound of claim 2 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

each R a is independently hydrogen, halogen, unsubstituted or substituted C 1 -C 4 alkyl, unsubstituted or substituted C 1 -C 4 fluoroalkyl, unsubstituted or substituted C 1 -C 4 heteroalkyl, —CN, —OH, —OR 14 , —CO 2 R 15 , —CH 2 CO 2 R 15 , —C(═O)N(R 15 ) 2 , —CH 2 C(═O)N(R 15 ) 2 , —N(R 15 ) 2 , or —CH 2 N(R 15 ) 2 ; and

each R b is independently hydrogen, halogen, unsubstituted or substituted C 1 -C 4 alkyl, unsubstituted or substituted C 1 -C 4 heteroalkyl, —CN, or —O-(unsubstituted or substituted C 1 -C 4 alkyl).

5. The compound of claim 2 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

each R a is independently hydrogen, F, Cl, Br, —CH 3 , —CH 2 CH 3 , —CH 2 CH 2 CH 3 , —CH(CH 3 ) 2 , —CH 2 CH 2 CH 2 CH 3 , —CH 2 CH(CH 3 ) 2 , —CH(CH 3 )(CH 2 CH 3 ), —C(CH 3 ) 3 , —CH 2 OH, —CH 2 CN, —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , —OCH 2 CH 3 , —OCF 3 , —CH 2 CH 2 OH, —CO 2 H, —CO 2 CH 3 , —CO 2 CH 2 CH 3 , —CH 2 CO 2 H, —CH 2 CO 2 CH 3 , —CH 2 CO 2 CH 2 CH 3 , —C(═O)NH 2 , —C(═O)NHCH 3 , —C(═O)N(CH 3 ) 2 , —CH 2 C(═O)NH 2 , —CH 2 C(═O)NHCH 3 , —CH 2 C(═O)N(CH 3 ) 2 , —NH 2 , —NHCH 3 , —N(CH 3 ) 2 , —CH 2 NH 2 , —CH 2 NHCH 3 , or —CH 2 N(CH 3 ) 2 ;

each R b is independently hydrogen, F, Cl, Br, —CH 3 , —CH 2 CH 3 , —CH 2 CH 2 CH 3 , —CH(CH 3 ) 2 , —CH 2 CH 2 CH 2 CH 3 , —CH 2 CH(CH 3 ) 2 , —CH(CH 3 )(CH 2 CH 3 ), —C(CH 3 ) 3 , —CH 2 OH, —CH 2 CN, —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , —OCH 2 CH 3 , or —OCF 3 .

6. The compound of claim 1 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

each R c is independently hydrogen, halogen, unsubstituted or substituted C 1 -C 4 alkyl, unsubstituted or substituted C 1 -C 4 fluoroalkyl, —CN, —OH, —OR 14 , —CO 2 R 15 , —CH 2 CO 2 R 15 , —C(═O)N(R 15 ) 2 , —NR 15 C(═O)NR 15 OR 14 , —C(═O)NR 15 OR 15 , —CH 2 C(═O)N(R 15 ) 2 , —N(R 15 ) 2 , —CH 2 N(R 15 ) 2 , —CH(CF 3 )N(R 15 ) 2 , —NR 15 C(═O)R 14 , —CH 2 NR 15 C(═O)R 14 , —SR 14 , —S(═O)R 14 , —SO 2 R 14 , —SO 2 N(R 15 ) 2 , or N(R 15 )SO 2 R 14 ; and

R d is independently hydrogen, halogen, unsubstituted or substituted C 1 -C 4 alkyl, unsubstituted or substituted C 1 -C 4 fluoroalkyl, unsubstituted or substituted monocyclic 4-7-membered heterocycle, —CN, —OH, —O-(unsubstituted or substituted C 1 -C 4 alkyl), —O-(unsubstituted or substituted C 1 -C 4 heteroalkyl), —C(═O)R 15 , —OC(═O)R 15 , —CO 2 R 15 , —CH 2 CO 2 R 15 , —C(═O)N(R 15 ) 2 , —OC(═O)N(R 15 ) 2 , —NR 15 C(═O)N(R 15 ) 2 , —NR 15 C(═O)OR 14 , —NR 15 C(═O)NR 15 OR 14 , —C(═O)NR 15 OR 15 , —CH 2 C(═O)N(R 15 ) 2 , —N(R 15 ) 2 , —CH 2 N(R 15 ) 2 , —CH(CF 3 )N(R 15 ) 2 , —NR 15 C(═O)R 14 , —CH 2 NR 15 C(═O)R 14 , —SO 2 N(R 15 ) 2 , —C(═NOR 15 )R 15 , —N(R 15 )SO 2 R 14 , —C(═O)NR 15 S(═O) 2 R 14 , —S(═O) 2 NR 15 C(═O)R 14 , or —C(═NR 15 )N(R 15 ) 2 ;

or if one R c and one R d are on adjacent atoms of ring B then the adjacent R c and R d groups are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted 5- or 6-membered monocyclic carbocycle or an unsubstituted or substituted 5- or 6-membered monocyclic heterocycle.

7. The compound of claim 1 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

each R c is independently hydrogen, F, Cl, Br, —CH 3 , —CH 2 CH 3 , —CH 2 CH 2 CH 3 , —CH(CH 3 ) 2 , —CH 2 CH 2 CH 2 CH 3 , —CH 2 CH(CH 3 ) 2 , —CH(CH 3 )(CH 2 CH 3 ), —C(CH 3 ) 3 , —CH 2 OH, —CH 2 CN, —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , —OCH 2 CH 3 , —OCF 3 , —CO 2 H, —CO 2 CH 3 , —CO 2 CH 2 CH 3 , —CH 2 CO 2 H, —CH 2 CO 2 CH 3 , —CH 2 CO 2 CH 2 CH 3 , —C(═O)NH 2 , —C(═O)NHCH 3 , —C(═O)NHOCH 3 , —C(═O)N(CH 3 ) 2 , —SO 2 N(CH 3 ) 2 , —C(═NOH)H, —C(═NOCH 3 )H, —CH 2 C(═O)NH 2 , —CH 2 C(═O)NHCH 3 , —CH 2 C(═O)N(CH 3 ) 2 , —NH 2 , —NHCH 3 , —N(CH 3 ) 2 , —NHCO 2 CH 3 , —NHSO 2 CH 3 , —CH 2 NH 2 , —CH 2 NHCH 3 , —CH 2 N(CH 3 ) 2 , CH(CF 3 )NH 2 , azetidinyl, or pyrrolidinyl;

each R d is independently hydrogen, F, Cl, Br, —CH 3 , —CH 2 CH 3 , —CH 2 CH 2 CH 3 , —CH(CH 3 ) 2 , —CH 2 CH 2 CH 2 CH 3 , —CH 2 CH(CH 3 ) 2 , —CH(CH 3 )(CH 2 CH 3 ), —C(CH 3 ) 3 , —CH 2 OH, —CH 2 CN, —CH 2 F, —CHF 2 , —CF 3 , pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, —CN, —OH, —OCH 3 , —OCH 2 CH 3 , —OCF 3 , —OCH 2 OCH 3 , —OCH 2 OCH 2 CH 3 , —OCH 2 CH 2 OH, —C(═O)NHOCH 3 , —C(═NOH)H, —C(═NOCH 3 )H, —CH 2 C(═O)NH 2 , —NH 2 , NHCO 2 CH 3 , NHSO 2 CH 3 , NH(C═O)NHCH 3 , NH(C═O)NHOCH 3 , or CH(CF 3 )NH 2 ;

or if one R c and one R d are on adjacent atoms of ring B then the adjacent R c and R d groups are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted 5- or 6-membered monocyclic heterocycle.

8. The compound of claim 1 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

each R a is independently hydrogen, F, Cl, Br, —CH 3 , —CHF, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , —OCF 3 , or —CH 2 CH 2 OH;

each R b is independently hydrogen, F, Cl, Br, —CH 3 , —CHF, —CHF 2 , —CF 3 , —CN, —OCH 3 , or —OCF 3 ;

each R c is independently hydrogen, F, Cl, Br, —CH 3 , —CHF, —CHF 2 , —CF 3 , pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, —CN, —OH, —OCH 3 , —OCF 3 , —NH 2 , —C(═O)NH 2 , —CONHCH 3 , —C(═NOH)H, —C(═NOCH 3 )H, —SO 2 CH 3 , —SO 2 N(CH 3 ) 2 , azetidinyl, or pyrrolidinyl;

each R d is independently hydrogen, F, Cl, Br, —CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , —OCF 3 , —OCH 2 OCH 3 , —CH 2 OH, —OCH 2 CH 2 OH, —C(═O)NH 2 , —C(═O)NHOCH 3 , —NH 2 , —NHCO 2 CH 3 , —NH(C═O)NHOCH 3 , or CH 2 (C═O)NH 2 ;

or if one R c and one R d are on adjacent atoms of ring B then the adjacent R c and R d groups are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted 5-membered monocyclic heterocycle.

9. The compound of claim 1 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

R 1 hydrogen;

R 2 is hydrogen, unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted or substituted C 1 -C 6 fluoroalkyl, unsubstituted or substituted C 3 -C 6 cycloalkyl or substituted or unsubstituted C 2 -C 6 heterocycloalkyl;

or R 1 and R 2 are taken together with the nitrogen atom to which they are attached to form ring C that is an unsubstituted or substituted N-containing C 2 -C 6 heterocycloalkyl;

R 5 is selected from the group consisting of hydrogen, halogen, —OH, —OR 14 , —S(═O) 2 R 14 , —N(R 15 ) 2 , —CN, —C(═O)OR 15 , —C(═O)N(R 15 ) 2 , unsubstituted or substituted C 1 -C 6 alkyl, and unsubstituted or substituted C 1 -C 6 fluoroalkyl;

or R 2 and R 5 are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted 4- to 7-membered saturated N-containing heterocyclic ring.

10. The compound of claim 1 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

11. The compound of claim 10 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

R 1 hydrogen;

R 2 is hydrogen, —CH 3 , —CH 2 CH 3 , —CH 2 CH 2 OH, —CH 2 CH 2 OCH 3 , CH 2 CH 2 F, —CH 2 CH 2 NH 2 , —CH 2 CH 2 NHCH 3 , —CH 2 CH 2 N(CH 3 ) 2 , —CH 2 CH 2 CH 3 , —CH(CH 3 ) 2 , cyclopropyl, —CH 2 CH 2 CH 2 F, CH 2 CH 2 CH 2 OH, CH 2 CH 2 CH 2 OCH 3 , —CH 2 CH 2 CH 2 CH 3 , —CH 2 CH(CH 3 ) 2 , —CH(CH 3 )(CH 2 CH 3 ), —C(CH 3 ) 3 , cyclobutyl, cyclopentyl, cyclohexyl, oxetanyl, tetrahydrofuranyl, or tetrahydropyranyl;

or R 1 and R 2 are taken together with the nitrogen atom to which they are attached to form ring C that is an unsubstituted or substituted azetidinyl, unsubstituted or substituted pyrrolidinyl, unsubstituted or substituted piperidinyl, unsubstituted or substituted morpholinyl, unsubstituted or substituted thiomorpholinyl, unsubstituted or substituted piperazinyl, or unsubstituted or substituted azepanyl;

R 5 is hydrogen, F, Cl, Br, —OH, —OCH 3 , —NH 2 , —NHCH 3 , —N(CH 3 ) 2 , —OCH 2 CH 3 , —OCF 3 , —CH 3 , —CH 2 CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —C(═O)OCH 3 , —C(═O)NH 2 , —C(═O)NHCH 3 , or —C(═O)N(CH 3 ) 2 ;

or R 2 and R 5 are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted monocyclic 4- to 7-membered heterocyclic ring selected from unsubstituted or substituted azetidinyl, unsubstituted or substituted pyrrolidinyl, unsubstituted or substituted piperidinyl, unsubstituted or substituted morpholinyl, unsubstituted or substituted thiomorpholinyl, unsubstituted or substituted piperazinyl, or unsubstituted or substituted azepanyl.

12. The compound of claim 1 , wherein the compound has the following structure of Formula (AVb), or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof:

13. The compound of claim 12 , wherein the compound of Formula (AVb) has the one of the following structures, or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof:

14. The compound of claim 12 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

R 1 hydrogen;

R 2 is hydrogen, methyl, ethyl, 2-fluoroethyl, 2-hydroxyethyl, 2-methoxyethyl, n-propyl, i-propyl, cyclopropyl, 3-fluoropropyl, 3-methoxypropyl, n-butyl, i-butyl, sec-butyl, cyclobutyl, or tert-butyl, or oxetanyl;

R 5 is hydrogen, F, Cl, Br, —OH, —OCH 3 , —NH 2 , —NHCH 3 , —N(CH 3 ) 2 , —OCH 2 CH 3 , —OCF 3 , —CH 3 , —CH 2 CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —C(═O)OCH 3 , —C(═O)NH 2 , —C(═O)NHCH 3 , or —C(═O)N(CH 3 ) 2 ;

or R 2 and R 5 are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted monocyclic 4- to 7-membered heterocyclic ring selected from unsubstituted or substituted azetidinyl, unsubstituted or substituted pyrrolidinyl, unsubstituted or substituted piperidinyl, unsubstituted or substituted morpholinyl, unsubstituted or substituted thiomorpholinyl, unsubstituted or substituted piperazinyl, or unsubstituted or substituted azepanyl.

15. The compound of claim 12 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

R 1 hydrogen;

R 2 is hydrogen, methyl, ethyl, 2-fluoroethyl, 2-hydroxyethyl, 2-methoxyethyl, n-propyl, i-propyl, cyclopropyl, 3-fluoropropyl, 3-methoxypropyl, n-butyl, i-butyl, sec-butyl, cyclobutyl, tert-butyl, or oxetanyl;

R 5 is hydrogen, F, Cl, Br, —OH, —OCH 3 , —NH 2 , —NHCH 3 , —N(CH 3 ) 2 , —OCH 2 CH 3 , —OCF 3 , —CH 3 , —CH 2 CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —C(═O)OCH 3 , —C(═O)NH 2 , —C(═O)NHCH 3 , or —C(═O)N(CH 3 ) 2 ;

or R 2 and R 5 are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted monocyclic 4- to 7-membered heterocyclic ring selected from unsubstituted or substituted azetidinyl, unsubstituted or substituted pyrrolidinyl, unsubstituted or substituted piperidinyl, unsubstituted or substituted morpholinyl, unsubstituted or substituted thiomorpholinyl, unsubstituted or substituted piperazinyl, or unsubstituted or substituted azepanyl.

16. The compound of claim 12 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

R a is hydrogen, F, Cl, Br, —CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , —OCF 3 , —CH 2 OH or —CH 2 CH 2 OH;

R b is hydrogen, F, Cl, Br, —CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , or —OCF 3 ;

each R c is independently hydrogen, F, Cl, Br, —CH 3 , —CH 2 F, —CHF 2 , —CF 3 , pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, —CN, —OH, —OCH 3 , —OCF 3 , —NH 2 , —C(═O)NH 2 , —C(═NOH)H, —C(═NOCH 3 )H, —SO 2 CH 3 , —SO 2 N(CH 3 ) 2 , azetidinyl, or pyrrolidinyl;

each R d is independently hydrogen, F, Cl, Br, —CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , —OCF 3 , —OCH 2 OCH 3 , —CH 2 OH, —OCH 2 CH 2 OH, —C(═O)NH 2 , —C(═O)NHOCH 3 , —NH 2 , —NHCO 2 CH 3 , —NH(C═O)NHOCH 3 , or —CH 2 (C═O)NH 2 ;

R e is hydrogen, F, Cl, Br, —CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —OH, —OCH 3 , or —OCF 3 ;

R 1 hydrogen;

R 2 is hydrogen;

R 5 is hydrogen, F, Cl, Br, —OH, —OCH 3 , —NH 2 , —NHCH 3 , —N(CH 3 ) 2 , —OCH 2 CH 3 , —OCF 3 , —CH 3 , —CH 2 CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —CN, —C(═O)OCH 3 , —C(═O)NH 2 , —C(═O)NHCH 3 , or —C(═O)N(CH 3 ) 2 ;

or R 2 and R 5 are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted monocyclic 6-membered heterocyclic ring selected from unsubstituted or substituted piperidinyl, unsubstituted or substituted morpholinyl, unsubstituted or substituted thiomorpholinyl, or unsubstituted or substituted piperazinyl.

17. The compound of claim 12 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, wherein:

R a is hydrogen, F, Cl, —CH 3 , —CF 3 , —CN, —OH, —CH 2 OH, —CH 2 CH 2 OH, —OCH 3 , or —OCF 3 ;

R b is hydrogen, F, Cl, —CH 3 , —CF 3 , —CN, —OH, —OCH 3 , or —OCF 3 ;

each R c is independently hydrogen, F, Cl, —CH 3 , —CF 3 , —CN, —OH, —NH 2 , —OCH 3 , —OCF 3 , ——C(═O)NH 2 , —C(═NOH)H , or —C(═NOCH 3 )H;

each R d is independently hydrogen, F, Cl, —CH 3 , —CF 3 , —CN, —OH, —NH 2 , —OCH 3 , —OCF 3 ;

R 1 hydrogen;

R 2 is hydrogen;

R 5 is hydrogen;

or R 2 and R 5 are taken together with the intervening atoms to which they are attached to form an unsubstituted or substituted morpholinyl.

18. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, and at least one pharmaceutically acceptable excipient.

19. A method of modulating somatostatin receptor subtype 2 (SSTR2) activity in a mammal comprising administering a compound of claim 1 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, to the mammal.

20. A method of treating acromegaly, a neuroendocrine tumor, pain, or combinations thereof, in a mammal comprising administering a compound of claim 1 , or a pharmaceutically acceptable salt, solvate, diastereomeric mixture, or individual enantiomers thereof, to the mammal in need thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2017
From: ZHAO, JIAN; HAN, SANGDON; KIM, SUN HEE; WANG, SHIMIAO; ZHU, YUNFEI
To: CRINETICS PHARMACEUTICALS, INC.
Reel/Frame 043145/0246 →
Continuity (3)
Provisional Application 62362493 · Jul 14, 2016
Provisional Application 62411338 · Oct 21, 2016
Related Publication 20180016252A1 · Jan 18, 2018