FIELD: chemistry.
SUBSTANCE: invention relates to compounds of formula II where A is , B is B2, and R5 represents R5b; B2 is pyridinyl, wherein any pyridinyl B2 is optionally substituted with one or more groups independently selected from a halogen atom, (C1-C6)alkyl, -O(C1-C6)alkyl, -O(C1-C6)alkyl-O(C1-C6)alkyl, (C3-C7)cycloalkyl, (C1-C6)haloalkyl, -CN and 6-membered heteroaryl, wherein any 6-membered heteroaryl is optionally substituted with one or more than one (C1-C6)alkyl or (C1-C6)haloalkyl; R1 is phenyl, 5-membered heteroaryl or 6-membered heteroaryl, wherein any phenyl, 5-membered heteroaryl or 6-membered heteroaryl R1 is optionally substituted with one or more groups independently selected from a halogen atom, -CN, (C1-C6)alkyl and (C1-C6)haloalkyl; one of the R3b groups represents a halogen atom, -CN or (C1-C6)alkyl, and the other R3b groups are independently selected from H, (C1-C6)alkyl and (C1-C6)haloalkyl; R4 represents H, (C1-C6)alkyl or (C1-C6)haloalkyl; R5b represents and salts thereof.
EFFECT: compounds may be useful in the treatment of diseases and conditions mediated by A1 channels with transient receptor potential (TRPA1).
39 cl, 5 tbl, 201 ex
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Authors
Dates
2018-12-25—Published
2014-10-09—Filed