IP Library › Granted Patent US 10,421,771
Granted Patent B2
US 10,421,771 · App. 14/790,645 · Granted Sep 24, 2019

Substituted nucleosides, nucleotides and analogs thereof

Inventors: Leonid Beigelman (San Mateo, CA); Guangyi Wang (Carlsbad, CA); David Bernard Smith (San Mateo, CA); Jerome Deval (Pacifica, CA); Marija Prhavc (Encintas, CA)
Assignee: ALIOS BIOPHARMA, INC.
C07H19/06A61K45/06A61P31/16C07D405/04C07D405/14C07D473/18C07D473/34C07D487/04C07D493/04C07H19/00C07H19/10C07H19/12C07H19/14C07H19/16C07H19/20C07H19/207C12N9/127C12Y207/07048
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Quick Facts
Patent No.
US 10,421,771
App. No.
14/790,645
Granted
Sep 24, 2019
Kind
B2
Abstract

Disclosed herein are nucleosides, nucleotides and analogs thereof, pharmaceutical compositions that include one or more of nucleosides, nucleotides and analogs thereof, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a disease and/or a condition, including an infection from a paramyxovirus and/or an orthomyxovirus, with a nucleoside, a nucleotide and an analog thereof.

Claims (62)

1. A compound of Formula (I), or a pharmaceutically acceptable salt thereof:

wherein:

B 1A is an optionally substituted purine base or an optionally substituted pyrimidine base;

R 1A is selected from the group consisting of hydrogen, an optionally substituted acyl, an optionally substituted O-linked amino acid,

the dashed line (------) is absent;

R 2A is selected from the group consisting of an unsubstituted C 1-6 alkyl, a halogen-substituted C 1-6 alkyl, a hydroxy-substituted C 1-6 alkyl, an alkoxy-substituted C 1-6 alkyl and a sulfenyl-substituted C 1-6 alkyl;

R 3A is selected from the group consisting of OH, OC(═O)R″ A and an optionally substituted O-linked amino acid;

R 4A is fluoro;

R 5A is hydrogen;

R 6A and R 7A are each absent or independently selected from the group consisting of hydrogen, an optionally substituted C 1-24 alkyl, an optionally substituted C 2-24 alkenyl, an optionally substituted C 2-24 alkynyl, an optionally substituted C 3-6 cycloalkyl, an optionally substituted C 3-6 cycloalkenyl, an optionally substituted aryl, an optionally substituted heteroaryl, an optionally substituted aryl(C 1-6 alkyl), an optionally substituted *—(CR 15A R 16A ) p —O—C 1-24 alkyl, an optionally substituted *—(CR 17A R 18A ) q —O—C 1-24 alkenyl,

R 6A is

and R 7A is absent or hydrogen; or

R 6A and R 7A are taken together to form a moiety selected from the group consisting of an optionally substituted

and an optionally substituted

wherein the oxygens connected to R 6A and R 7A , the phosphorus and the moiety form a six-membered to ten-membered ring system;

R 8A is selected from the group consisting of absent, hydrogen, an optionally substituted aryl and an optionally substituted heteroaryl;

R 9A is selected from the group consisting of NR 30A R 31A , an optionally substituted N-linked amino acid and an optionally substituted N-linked amino acid ester derivative;

R 10A and R 11A are independently an optionally substituted N-linked amino acid or an optionally substituted N-linked amino acid ester derivative;

R 12A , R 13A and R 14A are each independently absent or hydrogen;

each R 15A , each R 16A , each R 17A and each R 18A are each independently selected from the group consisting of hydrogen, an optionally substituted C 1-24 alkyl and alkoxy;

R 22A and R 23A are each independently selected from the group consisting of hydrogen, an optionally substituted C 1-24 alkyl and an optionally substituted aryl;

R 24A is selected from the group consisting of hydrogen, an optionally substituted C 1-24 alkyl, an optionally substituted aryl, an optionally substituted —O—C 1-24 alkyl and an optionally substituted —O-aryl;

R 25A and R 29A are each independently selected from the group consisting of hydrogen, an optionally substituted C 1-24 alkyl and an optionally substituted aryl;

R″ A is an optionally substituted C 1-24 -alkyl;

m is 0 or 1;

p and q are each independently selected from the group consisting of 1, 2 and 3; and

Z 1A , Z 2A , Z 3A , Z 4A are each O.

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1A is

R 6A is absent or hydrogen; and R 7A is absent or hydrogen.

3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1A is an unsubstituted acyl.

4. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1A is

5. The compound of claim 4 , or a pharmaceutically acceptable salt thereof, wherein both R 6A and R 7A are

6. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein B 1A is

7. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 2A is a halogen-substituted C 1-6 alkyl.

8. The compound of claim 1 , wherein the compound of Formula (I) is selected from the group consisting of:

or a pharmaceutically acceptable salt of any of the foregoing.

9. A pharmaceutical composition comprising an effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent, excipient, or combination thereof.

10. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1A is

R 6A is

R 7A is absent or hydrogen; m is 0; and R 12A and R 13A are independently absent or hydrogen.

11. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1A is

R 6A is

R 7A is absent or hydrogen; m is 1; and R 12A , R 13A and R 14A are independently absent or hydrogen.

12. The compound of claim 3 , or a pharmaceutically acceptable salt thereof, wherein the unsubstituted acyl is —C(═O)R 39A wherein R 39A is selected from the group consisting of an unsubstituted C 1-12 alkyl, an unsubstituted C 2-12 alkenyl, an unsubstituted C 2-12 alkynyl, an unsubstituted C 3-8 cycloalkyl, an unsubstituted C 5-8 cycloalkenyl, an unsubstituted C 6-10 aryl, an unsubstituted heteroaryl, an unsubstituted heterocyclyl, an unsubstituted aryl(C 1-6 alkyl), an unsubstituted heteroaryl(C 1-6 alkyl) and an unsubstituted heterocyclyl(C 1-6 alkyl).

13. The compound of claim 12 , or a pharmaceutically acceptable salt thereof, wherein R 39A is an unsubstituted C 1-12 alkyl.

14. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein B 1A is an optionally substituted purine base.

15. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein B 1A is an optionally substituted pyrimidine base.

16. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein B 1A is

17. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein B 1A is

18. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein B 1A is

19. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 2A is a chloro-substituted C 1-6 alkyl.

20. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 2A is a fluoro-substituted C 1-6 alkyl.

21. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3A is OH.

22. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3A is —OC(═O)R″ A .

23. The compound of claim 22 , or a pharmaceutically acceptable salt thereof, wherein R″ A is an unsubstituted C 1-8 alkyl.

24. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 3A is an optionally substituted O-linked amino acid.

25. The compound of claim 1 , wherein the compound of Formula (I) is selected from the group consisting of:

or a pharmaceutically acceptable salt of any of the foregoing.

26. The compound of claim 1 , wherein the compound of Formula (I) is selected from the group consisting of:

or a pharmaceutically acceptable salt of any of the foregoing.

27. A pharmaceutical composition comprising an effective amount of

or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, diluent, excipient, or combination thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2015
From: BEIGELMAN, LEONID; WANG, GUANGYI; SMITH, DAVID BERNARD; DEVAL, JEROME; PRHAVC, MARIJA
To: ALIOS BIOPHARMA, INC.
Reel/Frame 036695/0540 →
Continuity (4)
Continuation 13721988 · Dec 20, 2012
Provisional Application 61579560 · Dec 22, 2011
Provisional Application 61613836 · Mar 21, 2012
Related Publication 20150315228A1 · Nov 5, 2015