IP Library › Granted Patent US 9,403,823
Granted Patent B2
US 9,403,823 · App. 14/655,605 · Granted Aug 2, 2016

Protein kinase inhibitors

Inventors: Gwénaël Cheve (Lunel, FR); Bénédicte Dayde-Cazals (Montpellier, FR); Bénédicte Fauvel (Montpellier, FR); Cédric Bories (Montpellier, FR); Abdelaziz Yasri (Castelnau le Lez, FR)
Assignee: ORIBASE PHARMA
C07D471/04A61K31/437C12Q1/6886G01N33/5023G01N33/573C12Q2600/106C12Q2600/158G01N2333/912
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Quick Facts
Patent No.
US 9,403,823
App. No.
14/655,605
Granted
Aug 2, 2016
Kind
B2
Abstract

The present invention relates to compounds of the following formula (I) and/or the pharmaceutically acceptable addition salts, solvates, enantiomers, diastereoisomers thereof, as well as mixtures thereof. The subject matter of the present invention thus also includes the preparation of compounds of formula (I), their uses, in particular in the inhibition of protein kinases which are implicated for example in numerous diseases such as cancers or immune system disorders.

Claims (69)

1. Compound of the following formula (I):

characterized in that,

R1 is C 1 -C 6 alkyl group, hydroxyl group, or NR4R5,

R4 and R5 are independently a hydrogen atom, and/or C 1 -C 6 alkyl group,

X is CH 2 , C(S) or C(O),

R2 is a hydrogen atom, a C 1 -C 6 alkyl group or a halogen atom,

Y is chosen from a group consisting of HNC(O), HNC(S), HNSO 2 , HNC(O)CH 2 , HNC(S)CH 2 , HNC(O)NH, HNC(S)NH, CH 2 NHC(O), C(O)NH and C(O)NHCH 2 , CH 2 NHC(S),

R3 is chosen from a group consisting of:

an aryl, mono or polysubstituted with:

a hydroxyl group,

a halogen atom,

a C 1 -C 6 alkyl-amine group,

a C 1 -C 6 alkoxy group,

an amine substituted by a heteroaryl said heteroaryl optionally monosubstituted by a methyl,

a C 1 -C 6 trifluoroalkoxy group,

a C 1 -C 6 alkyl group,

a C 1 -C 6 trifluoroalkyl group,

a heteroaryl group optionally monosubstituted by a methyl,

an aliphatic heterocycle, optionally substituted by a methyl group, a hydroxyl group, an amine group, —NHCH 3 , or —N(CH 3 ) 2 ,

a C 1 -C 6 alkyl substituted by a heterocycle, wherein said heterocycle is optionally substituted by a methyl group, a hydroxyl group, an amine group, —NHCH 3 , or —N(CH 3 ) 2 , or

the fragment:

a heteroaryl group,

a non-aromatic monosubstituted cyclic group,

and/or the pharmaceutically acceptable addition salts, solvates, enantiomers, diastereoisomers thereof, as well as mixtures thereof.

2. Compound according to claim 1 characterized in that,

X is CH 2 ,

R2 is an alkyl, or a halogen atom.

3. Compound according to claim 1 , characterized in that,

R1 is C 1 -C 6 alkyl, or —NHMe,

R2 is a methyl or a chlorine atom,

Y is HNC(O), HNC(O)CH 2 , HNC(O)NH, HNC(S)NH, C(O)NH, C(O)NHCH 2 , or CH 2 NHC(O),

R3 is chosen from a group consisting of:

a phenyl group mono substituted with a C 1 -C 6 trifluoroalkyl group, a C 1 -C 6 trifluoroalkoxy group, a C 1 -C 6 alkyl group, a halogen, or a thiazol group,

a phenyl group polysubstituted with a C 1 -C 6 trifluoroalkyl, a C 1 -C 6 alkyl-amine, and/or a hydroxyl group,

a pyridine group, optionally substituted with a C 1 -C 6 alkyl or a C 1 -C 6 trifluoroalkyl,

a non-aromatic cyclic group chosen between a cyclic C 3 -C 10 alkyl, substituted with a C 1 -C 6 alkyl and/or a C 1 -C 6 trifluoroalkyl, and

a fragment chosen from a group consisting of:

4. Compound according to claim 1 , characterized in that,

R1 is a methyl group or —NHMe,

R2 is a methyl group,

Y is HNC*(O), wherein C* is linked to R3 and

R3 is chosen from a group consisting of:

5. Compound according to claim 1 of general formula (II):

characterized in that,

R1 is a methyl group or —NHMe,

X is a CH 2 ,

R2 is methyl group,

Y is HNC*(O), wherein C* is linked to R3 and

R3 is chosen from a group consisting of:

6. Compound according to claim 1 , characterized in that R2 is an alkyl or a halogen atom and in that R1 is a hydroxyl group, the corresponding salt thereof, and/or X is C═O.

7. Compound according to claim 1 , characterized in that,

R1 is C 1 -C 6 alkyl, or NR 4 R 5 ,

X is CH 2 or C(O),

R2 is a hydrogen, an alkyl or a halogen atom,

Y is HNC*(O), wherein C* is linked to R3 or HNC(O)NH, and

R3 is chosen from a group consisting of:

a phenyl group mono substituted with a C 1 -C 6 trifluoroalkyl group, a C 1 -C 6 alkyl group,

a phenyl group polysubstituted with a C 1 -C 6 trifluoroalkyl and a C 1 -C 6 alkyl-amine,

a pyridine group, optionally substituted with a C 1 -C 6 trifluoroalkyl,

a fragment chosen from a group consisting of:

8. Pharmaceutical composition, characterized in that it contains, as active principle, a compound according to claim 1 and a pharmaceutical acceptable excipient.

9. Compound according to claim 1 wherein Y is HNC(O).

10. Compound according to claim 1 of general formula (II):

characterized in that,

R1 is a methyl group or —NHMe,

X is a CH 2 ,

R2 is methyl group,

Y is HNC*(O), wherein C* is linked to R3 and

R3 is chosen from a group consisting of:

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2015
From: CHEVÉ, GWÉNAËL; DAYDE-CAZALS, BÉNÉDICTE; FAUVEL, BÉNÉDICTE; BORIÈS, CÉDRIC; YASRI, ABDELAZIZ
To: ORIBASE PHARMA
Reel/Frame 036957/0216 →
Priority Claims (1)
FR 12 62932 · Dec 28, 2012 · national
Continuity (2)
Provisional Application 61747031 · Dec 28, 2012
Related Publication 20160009709A1 · Jan 14, 2016