IP Library › Granted Patent US 10,472,392
Granted Patent B2
US 10,472,392 · App. 15/423,469 · Granted Nov 12, 2019

Macrocyclic inhibitors of flaviviridae viruses

Inventors: Caroline Aciro (Bottisham, GB); Jean Yves Chiva (Essex, GB); David Kenneth Dean (Ware, GB); Adrian John Highton (Chelmsford, GB); Petr Jansa (San Mateo, CA); Andrew John Keats (Essex, GB); Linos Lazarides (London, GB); Richard Mackman (Millbrae, CA); Karine G. Poullennec (Essex, GB); Adam James Schrier (Redwood City, CA); Dustin Scott Siegel (San Carlos, CA); Victoria Alexandra Steadman (Essex, GB); Greg Watt (Bristol, GB)
Assignees: Gilead Sciences, Inc.; Cypralis Limited
C07K5/0202A61K38/12A61K39/05A61K39/29A61K45/06C07D487/08C07D498/08C07D498/18C07D498/22C07K5/02A61K38/00A61K38/15Y02A50/385Y02A50/387Y02A50/389Y02A50/391Y02A50/393Y02A50/395
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Quick Facts
Patent No.
US 10,472,392
App. No.
15/423,469
Granted
Nov 12, 2019
Kind
B2
Abstract

Provided are compounds of Formula I: and pharmaceutically acceptable salts and esters thereof. The compounds, compositions, and methods provided are useful for the treatment of virus infections, particularly hepatitis C infections.

Claims (35)

1. A compound of Formula I:

or a pharmaceutically acceptable salt, isotope, stereoisomer, mixture of stereoisomers, tautomer, ester or prodrug thereof, wherein:

A is CH 2 ;

A 1 is (C 2 -C 5 )alkenylene, wherein a sp 3 carbon atom of A 1 is optionally replaced by —O—, —S(O) n —, —NH— or —N((C 1 -C 4 )alkyl)-, and wherein a sp 3 or sp 2 carbon atom of A 1 is optionally substituted with one or more groups selected from the group consisting of halo, (C 1 -C 5 )alkyl, (C 2 -C 8 )alkenyl, (C 2 -C 8 )alkynyl, aryl, heterocycloalkyl, cycloalkyl, aryl(C 1 -C 4 )alkyl, cycloalkyl(C 1 -C 4 )alkyl, heterocycloalkyl(C 1 -C 4 )alkyl, arylheterocycloalkyl(C 1 -C 4 )alkyl, —OR 9 , —SR 9 , —S(O)R 9 , —S(O) 2 R 9 and —N(R 9 ) 2 ;

A 2 is —CH(R 8 )-heteroarylene, wherein A 2 is optionally substituted with one or more substituents selected from the group consisting of —OR 9 , —SR 9 , —S(O)R 9 , —S(O) 2 R 9 , —N(R 9 ) 2 , halo, halo(C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkoxy, cyano and (C 1 -C 8 )alkyl;

L 1 is —O—C(O);

X 1 is —NH— or —N(CH 3 )—;

R 1 and R 2 , when taken together with the carbon to which they are both attached, form —C(═O)—;

R 3 is H or (C 1 -C 4 )alkyl optionally substituted with halo, cyano, hydroxyl or (C 1 -C 4 )alkoxy;

R 4a and R 4b are independently H or (C 1 -C 5 )alkyl, wherein each R 4a and R 4b is optionally substituted with one or more substituents selected from the group consisting of cyano, —COOH, halo, hydroxyl, amino, (C 1 -C 5 )alkoxy, mono(C 1 -C 5 )alkylamino, di(C 1 -C 5 )alkylamino, aryl and heteroaryl;

R 5a and R 5b are independently H or (C 1 -C 5 )alkyl optionally substituted with one or more substituents selected from the group consisting of —N 3 , cyano, —COOH, halo, hydroxyl, amino, mono(C 1 -C 5 )alkylamino, di(C 1 -C 5 )alkylamino, (C 1 -C 5 )alkoxy, aryl and heteroaryl, or

R 5a and R 5b together form a spirocycle having Formula (a):

wherein one or more carbon ring atoms of Formula (a) is optionally replaced by a nitrogen, oxygen or sulfur atom, and wherein a ring atom of Formula (a) optionally has one or more substituents selected from the group consisting of oxo, ═N(C 1 -C 4 )alkoxy, halo, hydroxyl, —NH 2 , (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, —OC(O)R 9 , —C(O) 2 R 9 , and —S(O) 2 R 9 ;

R 6a and R 6b together form a spirocycle having Formula (a);

R 8 is H, (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, (C 2 -C 4 )alkenyl, (C 2 -C 4 )alkynyl, aryl, heteroaryl, heterocycloalkyl or cycloalkyl, wherein R 8 is optionally substituted with —OR, —N(R 9 ) 2 , —CON(R 9 ) 2 , or cyano;

each R 9 is independently H, (C 1 -C 4 )alkyl, halo(C 1 -C 4 )alkyl, (C 2 -C 4 )alkenyl or (C 2 -C 4 )alkynyl; and

m is 1, 2, 3, 4 or 5.

2. The compound of claim 1 , wherein A 1 is

3. The compound of claim 1 , wherein A 2 is —CH(R 8 )-quinolinylene.

4. The compound of claim 1 , wherein R 8 is methyl.

5. The compound of claim 1 , wherein R 3 is H or methyl; one of R 4a and R 4b is H and the other is methyl; and one of R 5a and R 5b is H and the other is isopropyl.

6. The compound of claim 1 , wherein R 3 is H or methyl; one of R 4a and R 4b is H and the other is methyl; one of R 5a and R 5b is H and the other is isopropyl; A 2 is —CH(R 8 )-quinolinylene; and R 8 is methyl.

7. The compound of claim 1 , wherein R 6a and R 6b together form

8. The compound of claim 1 , wherein:

A 1 is

A 2 is

R 3 is H or methyl;

R 4a is methyl;

one of R 5a and R 5b is H and the other is iso-propyl; and

R 6a and R 6b together form

9. A compound selected from:

10. A pharmaceutical composition comprising a compound of claim 1 or a pharmaceutically acceptable salt, isotope, stereoisomer, mixture of stereoisomers, tautomer, ester or prodrug thereof and a pharmaceutically acceptable excipient.

11. A pharmaceutical composition comprising a compound of claim 9 a pharmaceutically acceptable salt, isotope, stereoisomer, mixture of stereoisomers, tautomer, ester or prodrug thereof and a pharmaceutically acceptable excipient.

12. The pharmaceutical composition of claim 10 , further comprising at least one additional therapeutic agent selected from the group consisting of interferons, ribavirin, HCV NS3 protease inhibitors, HCV NS5a inhibitors, nucleoside or nucleotide inhibitors of HCV NS5B polymerase, non-nucleoside inhibitors of HCV NS5B polymerase, and TLR-7 agonists; or a mixture thereof.

13. The pharmaceutical composition of claim 12 , wherein the at least one additional therapeutic agent is ribavirin, telaprevir, boceprevir or sofosbuvir.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 7, 2018
From: STEADMAN, VICTORIA ALEXANDRA; POULLENNEC, KARINE G.; LAZARIDES, LINOS; ACIRO, CAROLINE; DEAN, DAVID KENNETH; KEATS, ANDREW JOHN; SIEGEL, DUSTIN SCOTT; SCHRIER, ADAM JAMES; MACKMAN, RICHARD; JANSA, PETER; WATT, GREG; HIGHTON, ADRIAN JOHN; CHIVA, JEAN YVES
To: GILEAD SCIENCES, INC.; SELCIA LTD.
Reel/Frame 046575/0840 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 6, 2018
From: STEADMAN, VICTORIA ALEXANDRA; POULLENNEC, KARINE G.; LAZARIDES, LINOS; ACIRO, CAROLINE; DEAN, DAVID KENNETH; KEATS, ANDREW JOHN; SIEGEL, DUSTIN SCOTT; SCHRIER, ADAM JAMES; MACKMAN, RICHARD; JANSA, PETR; WATT, GREG; HIGHTON, ADRIAN JOHN; CHIVA, JEAN YVES
To: GILEAD SCIENCES, INC.; SELCIA LTD.
Reel/Frame 046565/0596 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2018
From: SELCIA LIMITED
To: CYPRALIS LIMITED
Reel/Frame 046600/0057 →
Continuity (5)
Continuation 15094777 · Apr 8, 2016
Continuation 14719242 · May 21, 2015
Division 13913288 · Jun 7, 2013
Provisional Application 61657562 · Jun 8, 2012
Related Publication 20170190734A1 · Jul 6, 2017