New access to the one-pot solvent-free synthesis of 4,5-dihydro-pyrido[2,3-b][1,4]diazepines and 2,3-dihydro-benzo[b][1,4]diazepines by microwave irradiation
β Scribed by Shyamaprosad Goswami; Anita Hazra; Subrata Jana
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 120 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.148
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β¦ Synopsis
Abstract
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A series of diversely substituted pyridodiazepines and benzodiazepines have been synthesized in solvent and catalyst free microwave condition from aryl/heteroaryl diamines and Ξ²βaryl vinyl ketones. The yields of the reactions varied with the substituents attached to the aryl/heteroaryl diamines. This common protocol is equally effective for the synthesis of pyridodiazepines and benzodiazepines with pharmacological interest, though in case of pyridodiazepines required time is comparatively higher than benzodiazepines. J. Heterocyclic Chem., (2009).
π SIMILAR VOLUMES
A new series of 7 -aryl-4,5-dihydro-2-oxo-3H,8H-furo[3,4-b][1,4] diazepines were prepared. Their \({ }^{1} \mathrm{H}\) nmr spectra have been interpreted in terms of the interconversion of two pseudo-boat conformers. Molecular-dynamics simulations at different temperatures on this type of compounds