Soluble guanylate cyclase activators

Patent metadata

Field	Value
Publication number	US-9611278-B2
Application number	US-201415103140-A
Country	US
Kind code	B2
Filing date	Dec 5, 2014
Priority date	Dec 11, 2013
Publication date	Apr 4, 2017
Grant date	Apr 4, 2017

Abstract

A compound of Formula I or a pharmaceutically acceptable salt thereof, are capable of modulating the body's production of cyclic guanosine monophosphate (“cGMP”) and are generally suitable for the therapy and prophylaxis of diseases which are associated with a disturbed cGMP balance. The invention furthermore relates to processes for preparing compounds of Formula I, or a pharmaceutically acceptable salt thereof, for their use in the therapy and prophylaxis of the abovementioned diseases and for preparing pharmaceuticals for this purpose, and to pharmaceutical preparations which comprise compounds of Formula I or a pharmaceutically acceptable salt thereof.

First claim

What is claimed is:

1. A compound having structural Formula I, or a pharmaceutically acceptable salt thereof:

or a pharmaceutically acceptable salt thereof wherein:
X 1 and X 2 are each independently CR or N;
R is —H, halo or cyclopropyl;
R 1 is —H or —C 1-6 alkyl unsubstituted or substituted with one to three of —F;
R 2 is (a) —C 1-6 alkyl unsubstituted or substituted with:
(i) one to six of —F,
(ii) —C 3-6 cycloalkyl unsubstituted or substituted with one to three of —F, or
(iii) phenyl unsubstituted or independently substituted at each occurrence with one to three of halo, —CN, —CH 3 or —OCH 3 ;
(b) —C 3-6 cycloalkyl unsubstituted or substituted with one to three of —F, or

(c) phenyl unsubstituted or independently substituted at each occurrence with one to three of halo, —CN, —CH 3 or —OCH 3 ;
R 2a is —H or —C 1-3 alkyl unsubstituted or substituted with one to three of —F;
R 2b is —H or —C 1-2 alkyl unsubstituted or substituted with one to three of —F;
or R 2b is —H and R 2 and R 2a are joined together with the carbon to which they are both attached to represent
(a) —C 3-6 cycloalkyl unsubstituted or substituted with one to three of —F, or
(b) a 4 to 6 membered heterocycle comprised of carbons and one or two heteroatoms independently selected from N, O or S, wherein the heterocycle is unsubstituted or independently substituted at each occurrence with one to three of halo, —CN, —CH 3 or —OCH 3 ;

R 3 is —C 1-6 alkyl or —C 3-6 cycloalkyl;
R 4 is
(a) a 5-membered heteroaryl ring comprised of at least one and up to three carbon atoms, at least one and up to four N atoms, and optionally one O atom or one S atom;
(b) a 6-membered heteroaryl ring comprised of carbon atoms and one or two N atoms; or
(c) an 8 to 10 membered bicyclic heteroaryl ring system comprised of carbon atoms and one to two heteroatoms independently selected from N, O or S;

wherein R 4 is unsubstituted or substituted on an available carbon or nitrogen in the ring or ring system with R 6 ;
R 6 is selected from:
(a) halo,
(b) —C 1-6 alkyl unsubstituted or substituted with one to three of —F, or —C 3-6 cycloalkyl for example but not limited to:

(c) —C 1-6 alkyl substituted with —C 3-6 cycloalkyl, such that the cycloalkyl and the alkyl share a common carbon at the point of attachment to each other, wherein said attachment can be with any non-terminal carbon in the alkyl group, for example but not limited to:

(d) —C 3-6 cycloalkyl,
(e) —OC 1-6 alkyl,
(f) —C 2-6 alkenyl,
(g) —C(O)OC 1-4 alkyl,
(h) —C 1-6 alkyl-C(O)OH,
(i) —C 1-6 alkyl-C(O)OC 1-3 alkyl, or
(j) -CD 3 ;

R 5 is —H, —OR 7 or —NHR 7 ; and
R 7 is —H, —C 1-6 alkyl or —C 3-6 cycloalkyl.

2. The compound of claim 1 or a pharmaceutically acceptable salt thereof wherein: X 1 and X 2 are each independently CH or N,
R 1 is —H or —C 1-3 alkyl;
R 3 is —C 1-6 alkyl or —C 3-6 cycloalkyl; and
R 5 is —H, —OH or —NH 2 .

3. The compound according to claim 1 or a pharmaceutically acceptable salt thereof wherein R 2 is:
(a) —C 1-6 alkyl substituted with
(i) one to six of —F,
(ii) —C 3-6 cycloalkyl substituted with one to three of —F; or
(iii) phenyl independently substituted at each occurrence with one to three of halo, —CN, —CH 3 or —OCH 3 ,

(b) —C 3-6 cycloalkyl substituted with one to three of —F, or
(c) phenyl independently substituted at each occurrence with one to three of -halo, —CN, —CH 3 or —OCH 3 .

4. The compound according to claim 1 or a pharmaceutically acceptable salt thereof wherein R 3 is —C 1-3 alkyl or cyclopropyl.

5. The compound according to claim 1 or a pharmaceutically acceptable salt thereof wherein R 4 is a 5-membered heteroaryl ring selected from:

and R 6a is —H or R 6 .

6. The compound according to claim 1 or a pharmaceutically acceptable salt thereof wherein R 4 is

wherein one of X 3 , X 4 , X 5 , X 6 or X 7 is N and the others are CH; and R 6a is —H or R 6 .

7. The compound according to claim 1 or a pharmaceutically acceptable salt thereof wherein R 4 is

wherein one or two of X 8 , X 9 , X 10 or X 11 is N and the others are CH.

8. The compound of claim 1 or a pharmaceutically acceptable salt thereof wherein R 5 is —H, —OH or —NH 2 .

9. The compound of claim 1 or a pharmaceutically acceptable salt thereof wherein R 6 is: (a) —F or —Cl, (b) —C 1-6 alkyl, (c) —CF 3 , (d) —CH 2 —C 3-6 cycloalkyl, (e) —C 1-3 alkyl substituted with —C 3-4 cycloalkyl such that the cycloalkyl and the alkyl share a common carbon at the point of attachment to each other, (f) —C 3-6 cycloalkyl, (g) —OC 1-6 alkyl, (h) —C 2-4 alkenyl, (i) —C(O)OC 1-4 alkyl, (j) —C 1-4 alkyl-C(O)OH, (k) —C 1-4 alkyl-C(O)OCH 3 , or (l) -CD 3 .

10. The compound of claim 1 having the structural Formula Ia, or a pharmaceutically acceptable salt thereof:

11. The compound of claim 1 , having the structural Formula Ib or a pharmaceutically acceptable salt thereof:

12. The compound of claim 1 , which is:
4-Amino-5-(5-fluoropyridin-2-yl)-5-methyl-2-(1-methyl-6-(3,3,4,4,4-pentafluorobutyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one;
4-Amino-2-(6-((3,3-difluorocyclobutyl)methyl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-5-(5-fluoropyridin-2-yl)-5-methyl-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one;
4-Amino-5-(5-fluoropyridin-2-yl)-5-methyl-2-(1-methyl-6-(4,4,4-trifluorobutyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one;
4-Amino-5-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)-2-(6-(3,3,4,4,4-pentafluorobutyl)-1-trideuteriomethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one;
4-Amino-5-cyclopropyl-5-(1-methyl-1H-tetrazol-5-yl)-2-(6-(3,3,4,4,4-pentafluorobutyl)-1-trideuteriomethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one;
4-Amino-5-cyclopropyl-5-(5-cyclopropyl-1,3,4-oxadiazol-2-yl)-2-(6-(3,3,4,4,4-pentafluorobutyl)-1-trideuteriomethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one;
4-Amino-5-cyclopropyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)-2-(6-(3,3,4,4,4-pentafluorobutyl)-1-trideuteriomethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-5H-pyrrolo[2, 3-d]pyrimidin-6(7H)-one;
4-Amino-5-cyclopropyl-5-(5-cyclopropyl-1,3,4-oxadiazol-2-yl)-2-(1-methyl-6-(3,3,4,4,4-pentafluorobutyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one;
4-Amino-5-cyclopropyl-5-(1-methyl-1H-1,2,3-triazol-4-yl)-2-(6-(3,3,4,4,4-pentafluorobutyl)-1-trideuteriomethyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-5H-pyrrolo[2,3-d]pyrimidin-6(7H)-one;
4-Amino-5-cyclopropyl-5-(1-methyl-1H-1,2,3-triazol-4-yl)-2-(1-methyl

Assignees

• Merck Sharp & Dohme

Inventors

• Han Xiaoqing
• Whitehead Alan
• Raghavan Subharekha
• Groeper Jonathan
• Guo Jian
• Zhang Yong

Classifications

• A61P9/00

  Drugs for disorders of the cardiovascular system · CPC title

• A61P3/10

  for hyperglycaemia, e.g. antidiabetics · CPC title

• A61P7/02

  Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors · CPC title

• A61P13/12

  of the kidneys · CPC title

• A61K45/06

  Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title