REACTIONS OF NITRILES UNDER ACIDIC CONDITIONS .9. SYNTHESIS OF 6-AMINO-1-ARYLURACILS, 6-AMINO-1-ARYL-2-THIOURACILS AND 6-AMINO-1,3-DIARYL-2-THIOURACILS UNDER ACIDIC CONDITIONS
Cj. Shishoo et al., REACTIONS OF NITRILES UNDER ACIDIC CONDITIONS .9. SYNTHESIS OF 6-AMINO-1-ARYLURACILS, 6-AMINO-1-ARYL-2-THIOURACILS AND 6-AMINO-1,3-DIARYL-2-THIOURACILS UNDER ACIDIC CONDITIONS, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 35(7), 1996, pp. 662-668
6-Amino-1-aryluracils (11a-g), 6-amino-1-aryl-2-thiouracils (12a-g), a
nd 6-amino-1,3-diaryl-2-thiouracils (6a,b) have been synthesised throu
gh the dry hydrogen chloride gas-catalysed condensation of ethyl cyano
acetate (7) with appropriate arylureas and thioureas. 1-Aryl (12a-g) a
rid 1,3-diaryl-2-thiouracils (6c-g) have been converted to the corresp
onding 1-aryl (15a-g) and novel hitherto unreported, 1,3-diaryluracils
(5a-e) through their oxidative desulphurisation.