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Efficient Synthesis of 6-(1H-1,2,4-Triazol-1-yl)-thieno[2,3-d]pyrimidin-4(3H)-ones via an Iminophosphorane.

Authors :
Sun, Yong
Huang, Nian-Yu
Ding, Ming-Wu
Source :
Synthetic Communications; 2010, Vol. 40 Issue 13, p1985-1991, 7p, 2 Diagrams, 1 Chart
Publication Year :
2010

Abstract

Ethyl 2-amino-4-methyl-5-(1H-1,2,4-triazol-1-yl)thiophene-3-carboxylate 2, obtained from Gewald reaction of 1-(1H-1,2,4-triazol-1-yl)acetone 1 with ethyl cyanoacetate and sulfur, was transferred into iminophosphorane 3. Further reaction of 3 with aromatic isocyanates gave carbodiimides 4, which were treated subsequently with a secondary amine to give 6-(1H-1,2,4-triazol-1-yl)-thieno[2,3-d]pyrimidin-4(3H)-ones 6 in good yields in the presence of a catalytic amount of sodium ethoxide. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00397911
Volume :
40
Issue :
13
Database :
Complementary Index
Journal :
Synthetic Communications
Publication Type :
Academic Journal
Accession number :
51311948
Full Text :
https://doi.org/10.1080/00397910903219351