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Preparaton of 6-oxo-and 6-thioxo-5, 6-dihydrobenzimidazo [1,2-c] quinazolines

✍ Scribed by A. L. L. Poot; J. F. Willems; F. C. Heugebaert


Publisher
Wiley (John Wiley & Sons)
Year
2010
Weight
323 KB
Volume
72
Category
Article
ISSN
0037-9646

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✦ Synopsis


Abstract

Substituted 6‐oxo‐and 6‐thioxo‐5, 6‐dihydrobenzimidazo [1,2‐c] quinazo‐lines were prepared by cyclization of 5(6) and 4(7) substituted 2‐(o‐aminophenyl) benzimidazoles with chloroethyl formate respectively with carbon disulphide.

The 5(6) and 4(7) substituted 2‐(o‐aminophenyl) benzimidazoles were prepared by reductive cyclization of the 4′ and 6′ substituted 2, 2′‐dinitroben‐zanilides which in their turn were obtained from o‐nitrobenzoyl chloride and 4 or 6 substituted o‐nitroanilines.


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ChemInform Abstract: Synthesis and Excha
✍ C. A. BATTY; M. K. MANTHEY; J. KIRK; M. MANTHEY; R. I. CHRISTOPHERSON; T. HAMBLE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Synthesis and Exchange Reactions of 5-Alkyl-2-oxo-6-thioxo-1,2,3,6-Tetrahydropyrimidine-4-carboxylic Acids. -The title compounds are prepared as potential dihydroorotase inhibitors. H/D-exchange studies establish a high tendency towards epimerization at C-5. No epimerization is observed under physi