Novel human nk₃ receptor-selective antagonist compounds, method for obtaining them and pharmaceutical compositions containing them

摘要

Cpds. of formula (I) B-(CH2)3-C(R1)(Ar1)-CH2-N(R2)-T-A-Z are new. In (I), R1 =H; R2 = Me; or R1+R2 = -(CH2)3- or -(CH2)4-; Ar1 = phenyl (opt. substd by halo, OH, 1-4C alkoxy, 1-4C alkyl, CF3 etc.); T = methylene, CO, COO, CONR3; R3 = H or 1-4C alkyl; A = direct bond, -CH2)t- or vinylene; or -T-A- = SO2; t = 1-3; Z = mono- di- or tricyclic aromatic or opt. substd. heteroaromatic gp.; B = e.g. gp. of formula (i) or (ii): J1 = e.g. Ar2-(CH2)x-C(X1), Ar2-CH=C, Ar2-CO-CH etc.; x = 0 or 1; Ar2 = phenyl (opt. substd.), pyridyl, thienyl, pyrimidyl, imidazolyl; X1 = e.g. 1-7C alkyl, formyl, 1-7C alkyl carbonyl, -(CH2)m-OR4 etc.; m = 0-2; R4 = H or 1-7C alkyl; and J2 = e.g. Ar2-N, Ar2-CH2-N, Ar2CO-N, Ar2CHOH-N etc.