Synthesis of 4-styryl-2,3-dihydro-1H-1,5-benzodiazepin-2-ones
โ Scribed by Z. F. Solomko; A. A. Gaponov; V. I. Avramenko; M. P. Khmel'
- Publisher
- Springer US
- Year
- 1987
- Tongue
- English
- Weight
- 265 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
โฆ Synopsis
UDC 547.892.07:543. 422.25'51 4-Styryl-2,3-dihydro-iH-l,5-benzodiazepin-2-ones were synthesized and their structure was established by means of PMR spectra and mass spectroscopy.
There is no unequivocal information on the structure of the reaction products of 4methyl-2,3-dihydro-iH-l,5-benzodiazepin-2-ones (Ia-d) with aromatic aldehydes. It was shown in [1-3] that it is not the methylene group but the methyl group that enters the reaction to form 4-styryl-2,3-dihydro-IH-l,5-benzodiazepin-2-one (IIa). Recently [4], it was reported that, according to certain chemical transformations, compounds IIe, g are 3-arylidene derivatives III. However, the authors did not prove the structure of the compounds obtained.
๐ SIMILAR VOLUMES
In the title compound, C 11 H 14 N 2 O, the diazepine ring adopts a skewed boat conformation. The molecule is stabilized by N-Hร ร รO intermolecular hydrogen bonds, forming a zigzag chain parallel to the b axis.