| 摘要 |
Thiazolidine derivs. (I; R1 = / ≠ R2 = C1-C8 alkyl, C3-C8 cycloalkyl, C3-C6 alkenyl, etc., R3 = H, C1-C4 alkyl, R4 = / ≠ R5 = C1-C6 alkyl, C3-C8 cycloalkyl, C3-C6 alkenyl, etc.) and their pharmaceutically acceptable salts for diuretic and saliuretic, were prepd. by reacting II with thiourea (III) to give I, treating I with acids to convert to their acid salts, or reacting their acid salts with base to convert to the free basic compd.
|
