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

Citation
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
Citations number
26
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
03764699
Volume
35
Issue
7
Year of publication
1996
Pages
662 - 668
Database
ISI
SICI code
0376-4699(1996)35:7<662:RONUAC>2.0.ZU;2-O
Abstract
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.