METHYLQUINAZOLIN-4-YLIDENECYANOACETIC ACID ETHYL ESTER
Muborak Azimovna TULYASHEVAInstitute of Pharmaceutical Education and Research Building 46, Yunusabad-19, Tashkent city, Uzbekistan,
ABI
Abstract
From a theoretical point of view, the 2,4-substituted quinazolines studied by us canexist in three (A, B, C) interconvertible tautomeric forms, and the reaction productcan be one of the most stable forms or a mixture of tautomers [1].In addition, for theB and C forms, one can write two geometric isomers, respectively, B' and C':
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