Synthesis and some properties of 1-(N-Nitrosoalkylamino)benzimidazoles
β Scribed by Alexander F. Pozharskii; Olga V. Dyablo; Alexander V. Belyaev; Zoya A. Starikova; Alexander I. Yanovskii
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 507 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
I-(N-N itrosoalkylamino)benzimidazoles (7a-e) were prepared by nitrosation of the parent amines with nitrous acid. The NMR data revealed 7a-d in solutions as mixtures of E and Z-isomers due to hindea'ed rotation arotmd the N-NO bond. l-(N-Nitrosoisopropylamino)benzimidazole (Te) existed in solutions as a sole Z-isomer. The rotation barrier around the N-NO bond was estimated for 7a by IH NMR dynamic spectroscopy. The molecular structure of l-fN-nitrosomethylammo)-2-rnethylbezimidazole (7d) was confn'med by X-ray structural data.
π SIMILAR VOLUMES
Thermolysis of N-phenylbenzamide oximes I, II and III (R = Cl, NO 2 and OCH 3 ) under nitrogen gives rise to benzimidazoles as the major products (45-52%), in addition to benzonitrile, arylamines, benzoic acid, phenols, benzanilides, 2-phenyl benzoxazoles and carbazoles. In the presence of naphthale