Compounds for treating spinal muscular atrophy

Patent metadata

Field	Value
Publication number	US-9371336-B2
Application number	US-201314380385-A
Country	US
Kind code	B2
Filing date	Feb 28, 2013
Priority date	Mar 1, 2012
Publication date	Jun 21, 2016
Grant date	Jun 21, 2016

Abstract

Provided herein are compounds, compositions thereof and uses therewith for treating spinal muscular atrophy.

First claim

What is claimed is:

1. A compound of Formula (IIa1) or Formula (IIIa1), respectively:

or a free acid, free base, salt, stereoisomer, racemate, enantiomer, diastereomer or tautomer thereof, wherein
R 1 is heterocyclyl optionally substituted with one, two or three R 3 substituents and optionally, with one additional R 4 substituent, or optionally substituted with one, two, three or four R 3 substituents;
R 2 is heteroaryl optionally substituted with one, two or three R 6 substituents and optionally, with one additional R 7 substituent;
R a is hydrogen;
R b is hydrogen;
R 3 is, in each instance, independently selected from cyano, halogen, hydroxy, oxo, C 1-8 alkyl, halo-C 1-8 alkyl, C 1-8 alkyl-carbonyl, C 1-8 alkoxy, halo-C 1-8 alkoxy, C 1-8 alkoxy-C 1-8 alkyl, C 1-8 alkoxy-carbonyl, amino, C 1-8 alkyl-amino, (C 1-8 alkyl) 2 -amino, amino-C 1-8 alkyl, C 1-8 alkyl-amino-C 1-8 alkyl, (C 1-8 alkyl) 2 -amino-C 1-8 alkyl, amino-C 1-8 alkyl-amino, C 1-8 alkyl-amino-C 1-8 alkyl-amino, (C 1-8 alkyl-amino-C 1-8 alkyl) 2 -amino, (C 1-8 alkyl) 2 -amino-C 1-8 alkyl-amino, [(C 1-8 alkyl) 2 -amino-C 1-8 alkyl] 2 -amino, (C 1-8 alkyl-amino-C 1-8 alkyl)(C 1-8 alkyl)amino, [(C 1-8 alkyl) 2 -amino-C 1-8 alkyl](C 1-8 alkyl)amino, C 1-8 alkoxy-C 1-8 alkyl-amino, (C 1-8 alkoxy-C 1-8 alkyl) 2 -amino, (C 1-8 alkoxy-C 1-8 alkyl)(C 1-8 alkyl)amino, C 1-8 alkyl-carbonyl-amino, C 1-8 alkoxy-carbonyl-amino, hydroxy-C 1-8 alkyl, hydroxy-C 1-8 alkoxy-C 1-8 alkyl, hydroxy-C 1-8 alkyl-amino, (hydroxy-C 1-8 alkyl) 2 -amino or (hydroxy-C 1-8 alkyl)(C 1-8 alkyl)amino;
R 4 is C 3-14 cycloalkyl, C 3-14 cycloalkyl-C 1-8 alkyl, C 3-14 cycloalkyl-amino, aryl-C 1-8 alkyl, aryl-C 1-8 alkoxy-carbonyl, aryl-sulfonyloxy-C 1-8 alkyl, heterocyclyl or heterocyclyl-C 1-8 alkyl; wherein, each instance of C 3-14 cycloalkyl, aryl and heterocyclyl is optionally substituted with one, two or three R 5 substituents;
R 5 is, in each instance, independently selected from halogen, hydroxy, cyano, nitro, C 1-8 alkyl, halo-C 1-8 alkyl, C 1-8 alkoxy, halo-C 1-8 alkoxy, amino, C 1-8 alkyl-amino, (C 1-8 alkyl) 2 -amino or C 1-8 alkyl-thio;
R 6 is, in each instance, independently selected from halogen, hydroxy, cyano, nitro, C 1-8 alkyl, C 2-8 alkenyl, halo-C 1-8 alkyl, hydroxy-C 1-8 alkyl, C 1-8 alkoxy, halo-C 1-8 alkoxy, C 1-8 alkoxy-C 1-8 alkyl, amino, C 1-8 alkyl-amino, (C 1-8 alkyl) 2 -amino or C 1-8 alkyl-thio; and,
R 7 is C 3-14 cycloalkyl, C 3-14 cycloalkyl-oxy, aryl, heterocyclyl or heteroaryl.

2. The compound of claim 1 , wherein the salt form is a chloride, hydrobromide, hydrochloride, dihydrochloride, acetate, trifluoroacetate or trifluoroacetic acid salt.

3. The compound of claim 1 , wherein the compound is selected from the group consisting of:
3-(1,3-benzothiazol-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzothiazol-2-yl)-7-(4-methylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzothiazol-2-yl)-7-[4-(2-chloroethyl)piperazin-1-yl]-2H-pyrano[2,3-b]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-(4-methylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-[4-(2-hydroxybenzyl)piperazin-1-yl]-2H-pyrano[2,3-b]pyridin-2-one
tert-butyl 4-[3-(1,3-benzothiazol-2-yl)-2-oxo-2H-pyrano[3,2-c]pyridin-7-yl]piperazine-1-carboxylate
tert-butyl 4-[3-(4-chloro-1,3-benzothiazol-2-yl)-2-oxo-2H-pyrano[3,2-c]pyridin-7-yl]piperazine-1-carboxylate
3-(4-chloro-1,3-benzothiazol-2-yl)-7-(piperazin-1-yl)-2H-pyrano[3,2-c]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-[4-(2-hydroxyethyl)piperazin-1-yl]-2H-pyrano[2,3-b]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-(4-methylpiperazin-1-yl)-2H-pyrano[3,2-c]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-(4-ethylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-(4-propylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzothiazol-2-yl)-7-(4-methylpiperazin-1-yl)-2H-pyrano[3,2-c]pyridin-2-one
3-(4-methyl-1,3-thiazol-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
7-(piperazin-1-yl)-3-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzothiazol-2-yl)-7-(4-ethylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzothiazol-2-yl)-7-(4-propylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzothiazol-2-yl)-7-[4-(propan-2-yl)piperazin-1-yl]-2H-pyrano[2,3-b]pyridin-2-one
7-(4-ethylpiperazin-1-yl)-3-(4-methyl-1,3-thiazol-2-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(4-methyl-1,3-thiazol-2-yl)-7-(4-propylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-[4-(2,3-dihydroxypropyl)piperazin-1-yl]-2H-pyrano[2,3-b]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-[4-(propan-2-yl)piperazin-1-yl]-2H-pyrano[2,3-b]pyridin-2-one
3-(6-methylimidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzothiazol-2-yl)-7-[4-(2-hydroxyethyl)piperazin-1-yl]-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzothiazol-2-yl)-7-[4-(2,3-dihydroxypropyl)piperazin-1-yl]-2H-pyrano[2,3-b]pyridin-2-one
3-(6-methylimidazo[1,2-a]pyridin-2-yl)-7-(4-methylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(imidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(7-methylimidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
7-(1,4-diazepan-1-yl)-3-(imidazo[1,2-a]pyrimidin-2-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-(1,4-diazepan-1-yl)-2H-pyrano[2,3-a]pyridin-2-one
7-(1,4-diazepan-1-yl)-3-(imidazo[2,1-b][1,3]thiazol-6-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(6-methylimidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[3,2-c]pyridin-2-one
3-(6-methylimidazo[1,2-a]pyridin-2-yl)-7-(4-methylpiperazin-1-yl)-2H-pyrano[3,2-c]pyridin-2-one
3-(8-chloro-6-methylimidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[3,2-c]pyridin-2-one
3-(imidazo[1,2-a]pyrimidin-2-yl)-7-(4-methyl-1,4-diazepan-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(4-chloro-1,3-benzothiazol-2-yl)-7-(4-methyl-1,4-diazepan-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(imidazo[1,2-a]pyridin-2-yl)-7-(4-methylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(7-methylimidazo[1,2-a]pyridin-2-yl)-7-(4-methylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(7-methylimidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[3,2-c]pyridin-2-one
3-(2-methylimidazo[2,1-b][1,3]thiazol-6-yl)-7-(piperazin-1-yl)-2H-pyrano[3,2-c]pyridin-2-one
3-(imidazo[1,2-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[3,2-c]pyridin-2-one
3-(5-methylpyrazolo[1,5-a]pyridin-2-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(imidazo[2,1-b][1,3]thiazol-6-yl)-7-(piperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
7-(1,4-diazepan-1-yl)-3-(imidazo[1,2-a]pyridin-2-yl)-2H-pyrano[2,3-b]pyridin-2-one
7-(1,4-diazepan-1-yl)-3-(8-fluoroimidazo[1,2-a]pyridin-2-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(8-chloroimidazo[1,2-a]pyridin-2-yl)-7-(1,4-diazepan-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(imidazo[1,2-a]pyridin-2-yl)-7-(4-methyl-1,4-diazepan-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(8-fluoroimidazo[1,2-a]pyridin-2-yl)-7-(4-methyl-1,4-diazepan-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(8-chloroimidazo[1,2-a]pyridin-2-yl)-7-(4-methyl-1,4-diazepan-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzothiazol-2-yl)-7-(1,4-diazepan-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(1,3-benzoxazol-2-yl)-7-(1,4-diazepan-1-yl)-2H-pyrano[2,3-b]pyridin-2-one
7-(4-methylpiperazin-1-yl)-3-(5-methylpyrazolo[1,5-a]pyridin-2-yl)-2H-pyrano[2,3-b]pyridin-2-one
3-(imidazo[2,1-b][1,3]thiazol-6-yl)-7-(4-methylpiperazin-1-yl)-2H-pyrano[2,3-b]pyridin-2-o

Assignees

• Ptc Therapeutics Inc
• Hoffmann La Roche
• Ptc Therapeutics Inc

Inventors

• Lee Chang-Sun
• Choi Soongyu
• Karp Gary Mitchell
• Koyama Hiroo
• Ratni Hasane

Classifications

• A61P43/00

  Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00 · CPC title

• A61P19/00

  Drugs for skeletal disorders · CPC title

• A61P21/00

  Drugs for disorders of the muscular or neuromuscular system · CPC title

• C07D491/052

  the oxygen-containing ring being six-membered · CPC title

• C07D491/04

  Ortho-condensed systems · CPC title