PROCESS FOR PRODUCING NEW ANTIALLERGIC AND ANTITHROMBOTICHETEROCYCLIC COMPOUNDS
Heterocycles of formula (I) and their pharmaceutically acceptable salts are new, Z = N W =CHR2 when n = 0 or CR2 or CHR2 when n = 1; Y = CH2O, OCH2, CH2S, SCH2, CH2N(R2), N(R2)CH2, CON(R2) or N(R2)CO; n = 0 or 1; R1 = H, lower alkyl, lower alkoxy, lower alkanoyl, halo, CF3, NO2 or CN; R2 = H or lowe...
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Zusammenfassung: | Heterocycles of formula (I) and their pharmaceutically acceptable salts are new, Z = N W =CHR2 when n = 0 or CR2 or CHR2 when n = 1; Y = CH2O, OCH2, CH2S, SCH2, CH2N(R2), N(R2)CH2, CON(R2) or N(R2)CO; n = 0 or 1; R1 = H, lower alkyl, lower alkoxy, lower alkanoyl, halo, CF3, NO2 or CN; R2 = H or lower alkyl; R3 = lower alkyl, lower perfluoroalkyl or perfluorophenyl, halo = F, Cl or Br; lower alkyl or alkoxy = 1-6C; lower alkanoyl = 2-6C. Specifically claimed are 3 cpds. (I) viz. N-(3-((2-quinolyl) methoxy)phenyl)ethane sulphonamide, N-(3-((2-quinolyl) methoxy) phenyl) -1-butanesulphonamide and N-(3-((2-quinolyl) methoxy) phenyl) trifluoromethane sulphonamide (Ia). |
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