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Synthesis of new 6‐Aroylpyrido[2,3‐ d ]pyrimidines
Author(s) -
Quiroga Jairo,
Viveros GermÁN,
Insuasty Braulio,
Nogueras Manuel,
Sánchez Adolfo,
Cobo Justo
Publication year - 1999
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570360228
Subject(s) - chemistry , dimethylformamide , hydrochloride , acetal , medicinal chemistry , organic chemistry , solvent
Abstract The synthesis of 6‐dimethylaminomethylenaminopyrimidin‐4(3 H )‐ones 2 and its reaction with β‐dimethyl‐aminopropiophenone hydrochloride 3 is discussed in this work. The reaction of 6‐aminopyrimidin‐4(3 H )‐ones 1 with an excess of dimethylformamide dimethyl acetal gives rise to the formation of 6‐dimethylaminomethyleneaminopyrimidines 2. The heating of equimolecular quantities of 2 and 3 in dimethylformamide leads to the 6‐aroylpyrido[2,3‐ d ]pyrimidines derivatives 4. The structures of compounds 2 and 4 were determined on the basis of nmr measurements.