Title of article :
Synthesis and Reactions of some 2-Vinyl-3H-quinazolin-4-ones
Author/Authors :
Anette Witt، نويسنده , , Martin Jan Bergman، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2000
Abstract :
A simple, high-yielding synthesis of 2-vinyl-3H-quinazolin-4-one, 2-(1-chlorovinyl)-3H-quinazolin-4-one and 2-(1-bromovinyl)-3H-quinazolin-4-one. The 2-vinylquinazolinones 11a and 14 participate readily in nucleophilic addition reactions. Treatment with both carbon and nitrogen nucleophiles results in a clean conversion into a variety of 2-substituted 3H-quinazolin-4-one derivatives. The 2-(1-halovinyl)-3H-quinazolin-4-ones 11b and 11c reacted with carbon nucleophiles to give several derivatives of 2-substituted 3H-quinazolin-4-one, such as dihydrofurancarboxylic ethyl ester 23.
Keywords :
Cyclisation , Michael reactions , quinazolinones
Journal title :
Tetrahedron
Journal title :
Tetrahedron