FIELD: pharmaceuticals.
SUBSTANCE: invention relates to compounds and pharmaceutically acceptable salts thereof, wherein in formula I-b ring A and B are phenyl; R1 is a reactive group -L-Y, where R1 is bonded to a ring A in a position other than an atom adjacent to the atom attached to W1, L and Y are as specified in the claim, W1 and W2 each represent -NR2-; R2 is hydrogen, C1-6 aliphatic group or -C(O)R; m and p are independently 0–4; Ry is halogen; Rx is independently selected from -R, -OR, -O(CH2)qOR, or halogen, where q is 1, 2, 3 or 4; and Rv is independently selected from -R, halogen, -OR, -O(CH2)qOR, -CN, -NO2, -SO2R, -SO2N(R)2, -SOR, -C(O)R, -CO2R, -C(O)N(R)2, -NRC(O)R, -NRC(O)N(R)2, -NRSO2R or -N(R)2, where q is 1–4. Invention also relates to compositions for inhibiting at least one kinase selected from BTK, TEC, BMX, ITK, ErbB1, ErbB2, ErbB3, ErbB4 and JAK3 or mutants thereof, methods of inhibiting said kinases and mutants thereof, as well as methods of treating disorders mediated by said kinases.
EFFECT: compounds of formula I-b as inhibitors of activity of at least one kinase selected from BTK, TEC, BMX, ITK, ErbB1, ErbB2, ErbB3, ErbB4 and JAK3 or mutants thereof.
47 cl, 25 dwg, 20 tbl, 286 ex
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Authors
Dates
2020-10-23—Published
2009-06-26—Filed