Azepinones. III. N-Oxidation and subsequent nitration of dibenzodiazepinone

Author:

Amiet RG,Johns RB

Abstract

Dibenzo[c,f]-[1,2]-diazepin-11-one (I) is converted under conditions favour- able for nitration into the N-oxide (IV), and this in turn nitrates readily to form 2-nitro- and 2,4-dinitrodibenzo[c,f]-[1,2]- diazepin-11-one-6-oxide the structures of which are proposed largely on spectroscopic evidence. The experimental results suggest that the heterocyclic ring in compound (I) has little tropone-like character.

Publisher

CSIRO Publishing

Subject

General Chemistry

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. 2-Nitrodiphenylalkanes/alkenes as adept photosynthons for direct access to valuable N-heterocycles;Journal of Photochemistry and Photobiology A: Chemistry;2019-04

2. Dibenzodiazepines and other Tricyclic Diazepine Systems;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02

3. Photolysis of acetyl esters of 2,2′-dinitrodiphenyl-carbinols in protic and aprotic solvents;Research on Chemical Intermediates;1991-06

4. Quaternary salts of 2H-imidazoles;Journal of the Chemical Society, Perkin Transactions 1;1983

5. In vivo studies on the metabolism of dibenzo [c,f]-[1,2] diazepine;European Journal of Drug Metabolism and Pharmacokinetics;1979-04

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