CYCLOCONDENSATION OF 2,4-DIAMINO-6(1H)PYRIMIDONE WITH ALPHA-OXOKETENEDITHIOACETALS - SYNTHESIS OF NOVEL 5-ALKYLTHIO-7-SUBSTITUTED AND 6,7-ANNULATED-5-DEAZAPTERIDINE DERIVATIVES
Sk. Sharma et al., CYCLOCONDENSATION OF 2,4-DIAMINO-6(1H)PYRIMIDONE WITH ALPHA-OXOKETENEDITHIOACETALS - SYNTHESIS OF NOVEL 5-ALKYLTHIO-7-SUBSTITUTED AND 6,7-ANNULATED-5-DEAZAPTERIDINE DERIVATIVES, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 32(11), 1993, pp. 1173-1175
Cyclocondensation of 2,4-diamino-6(1H)-pyridimine (1) with a variety o
f acyclic and cyclic oxoketene dithioacetals (2a-i) in refluxing aceti
c acid and piperidine affords the title (5-deazapteridines (3a-i) in m
oderate to excellent yields.