A four-component modified Biginelli reaction: A novel approach for C-2 functionalized dihydropyrimidines
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A novel four component modified Biginelli reaction for the synthesis of C-2 functionalized dihydropyrimidines has been established. The approach uses assembly of less explored acetyl acetone with aromatic aldehyde, thiourea, and dimethyl sulphate to construct a novel 5-acetyl 2-methylthio dihydropyrimidine system, which works as an efficient well-designed intermediate for generating C-2 modified Biginelli libraries with nitrogen nucleophiles. Phenyl hydrazine, semicarbazide, and aryl semicarbazides are successfully used as N-nucleophiles to generate C-2 functionalized dihydropyrimidine derivatives, which fulfil the demands of active pharmacophore. Time economy, step economy, and a single pot reaction with moderate to excellent yield are the major advantages of this novel method.
Nội dung trích xuất từ tài liệu:
A four-component modified Biginelli reaction: A novel approach for C-2 functionalized dihydropyrimidines
Nội dung trích xuất từ tài liệu:
A four-component modified Biginelli reaction: A novel approach for C-2 functionalized dihydropyrimidines
Tìm kiếm theo từ khóa liên quan:
Journal of Chemistry Biginelli reaction Green synthesis 4-MCR 2-Methylthio-1.4-DHPMs N-nucleophiles Phenyl hydrazineGợi ý tài liệu liên quan:
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