An expedient synthesis of 3-amino-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one
✍ Scribed by Mark G Bock; Robert M DiPardo; Ben E Evans; Kenneth E Rittle; Daniel F Veber; Roger M Freidinger
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 204 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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📜 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-HÁ Á ÁO intermolecular hydrogen bonds, forming a zigzag chain parallel to the b axis.
## 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