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Synthesis of 4-styryl-2,3-dihydro-1H-1,5-benzodiazepin-2-ones

โœ 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

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โœฆ 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.


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4,4-Dimethyl-4,5-dihydro-1H-1,5-benzodia
โœ Rashid, Naghmana ;Hasan, Mashooda ;Yusof, Nurdiyana M. ;Yamin, Bohari M. ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› International Union of Crystallography ๐ŸŒ English โš– 289 KB

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 รO intermolecular hydrogen bonds, forming a zigzag chain parallel to the b axis.