AN EFFICIENT IMINOPHOSPHORANE-MEDIATED SYNTHESIS FOR PYRIDO[3',2'4,5]THIENO[3,2-D] PYRIMIDINE-DERIVATIVES

Citation
C. Peinador et al., AN EFFICIENT IMINOPHOSPHORANE-MEDIATED SYNTHESIS FOR PYRIDO[3',2'4,5]THIENO[3,2-D] PYRIMIDINE-DERIVATIVES, Tetrahedron, 50(22), 1994, pp. 6705-6714
Citations number
36
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404020
Volume
50
Issue
22
Year of publication
1994
Pages
6705 - 6714
Database
ISI
SICI code
0040-4020(1994)50:22<6705:AEISFP>2.0.ZU;2-S
Abstract
A ready one-pat preparation for pyridothienopyrimidines bearing variou s substituents at position 2 of the pyrimidine ring is reported. The a za Wittig-type reaction of iminophosphoranes derived from the aldehyde 4 with heterocumulenes leads to functionalized fused pyrimidines. Imi nophosphoranes 6, nylphosphoranylidine)amino]thieno[2,3-b]pyridines, r eact with isocyanates, carbon dioxide and carbon disulfide under mild conditions to give the functionalized 3-dihydropyrido[3',2':4,5]thieno [3,2-d]pyrimidines 7, 8 and 9, respectively.