FIELD: organic chemistry, chemical technology. SUBSTANCE: invention relates to novel method of synthesis of compound of the formula (I) in each case in free form and as salt where Q means CH or N; Y means NO2 or CN; Z means CHR3, O, NR3 or S; R1 and R2 each means independently hydrogen atom, unsubstituted or R4-substituted C1-C8-alkyl or in common they form alkylene bridge consisting of two or three carbon atoms being alkylene bridge can comprise additionally heteroatom taken among group including NR5, O or S; R3 means H, unsubstituted or R4-substituted C1-C12-alkyl; R4 means unsubstituted or substituted aryl or heteroaryl; R5 means H or C1-C12-alkyl. Method involves conversion of compound of the formula (II) where R means cyclohexyl, phenyl, benzyl or group of the formula (a) ; X1 means group to be eliminated with halogenating agent to compound of the formula (IV) where X means halogen atom and conversion of synthesized compound of the formula (IV) to compound of the formula (VI) by interaction with compound of the formula (V) that is converted to compound of the formula (I) using chlorinating agent being in compound of the formula (IV) values R, X, X1 are indicated above. Invention relates also to method of synthesis of compound of the formula (IV) involving interaction of compound of the formula (II) with halogenating agent. EFFECT: improved method of synthesis of thiazole derivatives. 6 cl, 6 tbl, 16 ex
Authors
Dates
2002-10-27—Published
1997-12-17—Filed