Synthesis and pharmacological study of 1,3-dihydro-1,3-dimethyl-5-phenyl-7-nitro-2H-1,4-benzodiazepin-2-one
✍ Scribed by A. N. Grinev; É. S. Krichevskii; O. B. Romanova; A. I. Ermakov; I. K. Sokolov; M. D. Mashkovskii
- Book ID
- 112400665
- Publisher
- Springer
- Year
- 1983
- Tongue
- English
- Weight
- 375 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0091-150X
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## Abstract Two benzodiazepines, Diazepam and Flunitrazepam, labeled with carbon‐14 in position 5 of the diazepine ring have been synthesized. Use of a condensation between iminochlorides and ^14^C‐benzonitriles, followed by exhaustive methylation of the resulting quinazolines and hydrolyses is des
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-HÁ Á ÁO intermolecular hydrogen bonds, forming a zigzag chain parallel to the b axis.
## Abstract The synthesis from carbon‐^14^C dioxide of 1, 3‐dihydro‐1‐methyl‐7‐nitro‐5‐phenyl‐2H‐1, 4‐benzodiazepin‐2‐one‐5‐^14^C (I) for use in metabolic studies has been described. The synthesis was achieved by the sequence shown in figure 1. The overall yield of labelled nimetazepam (I) was near