CONJUGATE ADDITION OF NUCLEOPHILES TO THE VINYL FUNCTION OF 2-CHLORO-4-VINYLPYRIMIDINE DERIVATIVES

Conjugate Addition of Nucleophiles to the Vinyl Function of 2-Chloro-4-vinylpyrimidine Derivatives

Conjugate Addition of Nucleophiles to the Vinyl Function of 2-Chloro-4-vinylpyrimidine Derivatives

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Conjugate addition reaction fire resistant tablecloth of various nucleophiles across the vinyl group of 2-chloro-4-vinylpyrimidine, 2-chloro-4-(1-phenylvinyl)pyrimidine and 2-chloro-4-vinylquinazoline provides the corresponding 2-chloro-4-(2-substituted ethyl)pyrimidines and brynje tactical beanie 2-chloro-4-(2-substituted ethyl)quinazolines.Treatment of these products, without isolation, with N-methylpiperazine results in nucleophilic displacement of chloride and yields the corresponding 2,4-disubstituted pyrimidines and quinazolines.

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