Substituted sulfonylurea derivatives
AssigneeZydus Lifesciences Limited
InventorsRajiv Sharma, Sameer Agarwal
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Abstract
The present invention relates to novel heterocyclic compounds of the general formula (I) their pharmaceutically acceptable salts, pharmaceutically acceptable solvates, enantiomers, diastereomers and polymorphs. The invention also relates to processes for the preparation of the compounds of invention, pharmaceutical compositions containing the compounds and their use as the compounds of the invention belong to the family of NOD-like receptor family (NLR) protein NLRP3 modulators. The present invention thus relates to novel NLRP3 modulators as well as to the use of the novel inhibitor compounds in the treatment of diseases or conditions in which interleukin 1β activity is implicated.
Claims13
A compound having the structure of general formula (I)
- or a tautomeric form, a stereoisomer, an enantiomer, or a pharmaceutically acceptable salt, thereof,
- wherein,
- R1 at each occurrence is independently selected from hydrogen, halogen, haloalkyl, cyano, and optionally substituted groups selected from (C1-C6)alkyl, (C1-C6)haloalkyl, (C2-C6)alkenyl, (C1-C6)alkoxy, (C3-C7)cycloalkyl, NH2, NH(C1-C6)alkyl, N(C3-C7)cycloalkyl, N(C1-C6 alkyl)2, aryl, heteroaryl, heterocyclyl, benzyl, thiol, mercapto alkyl, SO2(C1-C6)alkyl, (C1-C6)thio-alkoxy, and amide;
- X is N—R5, O, S, or SO2;
- R5 at each occurrence is independently selected from hydrogen, halogen, haloalkyl, cyano, and optionally substituted groups selected from (C1-C6)alkyl, (C1-C6)haloalkyl, (C2-C6)alkenyl, (C2-C6)alkynyl, (C1-C6)alkoxy, (C3-C7)cycloalkyl, (C1-C6)alkylSO2(C1-C6)alkyl, (C1-C6)alkylN(C1-C6)alkyl, (C1-C6)alkylN(C3-C7)cycloalkyl, aryl, heteroaryl, heterocyclyl, benzyl, tert-butyloxycarbonyl, thiol, mercapto alkyl, SO2(C1-C6)alkyl, SO2(C3-C7)cycloalkyl, SO2-aryl, SO2-heterocyclyl, (C1-C6)thioalkyl, (C1-C6)thioalkoxy, (C1-C6)alkylSO2NH2, —CONH2, —CO(C1-C6)alkyl, —CO(C1-C6)haloalkyl, —CO-aryl, —CO-heteroaryl, —CO-heterocyclyl, 4- to 7-membered heterocyclic ring, 7- to 14-membered bicyclic heterocyclic ring system, and bridged or spiro ring system having optionally one or more than one heteroatoms;
- m and n is independently selected from integer 0-3;
- q and r is independently selected from integer 1-4;
- R2 at each occurrence is independently selected from hydrogen, halogen, cyano, and optionally substituted groups selected from (C1-C6)alkyl, (C2-C6)alkenyl, (C1-C6)alkoxy, (C3-C7)cycloalkyl, benzyl, aryl, heteroaryl, heterocyclyl, thiol, thioalkyl, thio-alkoxy, SO2(C1-C6)alkyl, SO(C1-C6)alkyl, and bridged or spiro ring system having optionally one or more than one heteroatoms;
- each of R3 and R4 at each occurrence is independently selected from hydrogen, halogen, haloalkyl, cyano, nitro, amide, sulphonamide, acyl, hydroxyl, and optionally substituted groups selected from (C1-C6)alkyl, (C1-C6)haloalkyl, (C3-C6)cycloalkyl, (C1-C6)alkoxy, SO2(C1-C6)alkyl, thiol, mercapto alkyl, benzyl, aryl, heteroaryl, and heterocyclyl;
- alternatively R3 and R4 forms a bond;
- ‘B’ is selected from the following ring systems
- wherein X, Y, Z at each occurrence are independently selected from C, N, S, SO2 and O, which may, wherever possible be optionally substituted;
- each of R6, R7, R8, R9, R10 and R11 at each occurrence are independently selected from hydrogen, halogen, cyano, amide, sulphonamide, acyl, hydroxyl, and optionally substituted groups selected from (C1-C6)alkyl, (C1-C6)haloalkyl, (C3-C6)cycloalkyl, (C1-C6)alkoxy, benzyl, aryl, heteroaryl, and heterocyclyl;
- alternatively each of R7 and R8, R8 and R9, R9 and R10 or R10 and R11 wherever possible, together may form a 4 to 7 membered saturated or partially saturated ring containing from 0-2 additional heteroatoms selected from the group consisting of N, O, and S(O)p;
- and
- p is 1 or 2.
Dependencies are inferred from the claim text.