95680-61-8

Usage

Chemical class

Diazepines

Substitution on the diazepine ring

1-benzoyl-5-methoxy-

Potential pharmacological activities

Acts as an agonist for certain receptors in the body

Potential applications

Development of novel drugs for various therapeutic purposes

Other properties of interest

Chemical and biological properties for further research and development in the pharmaceutical and chemical industries.

Upstream product

• 98-88-4 benzoyl chloride 
• 95680-57-2 5-methoxy-6H-1,4-diazepine 

Downstream Products

• 114913-59-6 1-benzoyl-5-methoxy-6,7-dihydro-1H-1,4-diazepine 
• 114913-58-5 2-benzoyl-3-methoxypyrrole 
• 95680-62-9 N-(6-methoxypyridin-3-yl)benzamide 

Relevant academic research and scientific papers

Studies on Diazepines. XXVI. Syntheses of 6H-1,4-Diazepines and 1-Acyl-1H-1,4-diazepines from 4-Pyridyl Azides

Photolysis of 4-azidopyridines (7a-e) in the presence of methoxide ions resulted in ring expansion to give 5-methoxy-6H-1,4-diazepines (10a-e), presumably via the azirine intermediates 8 derived from the initially formed singlet pyridylnitrenes.Treatment

PHOTOLYSIS OF PYRIDYL AZIDES IN THE PRESENCE OF METHOXIDE IONS: FORMATION OF FULLY UNSATURATED 1,3- AND 1,4-DIAZEPINES

Photolysis of 4-azidopyridines (1) in the presence of methoxide ions resulted in ring-expansion to give the 6H-1,4-diazepines (4).Treatment of the diazepine (4a) with benzoyl chloride afforded the 1-benzoyl-1H-1,4-diazepine (5), whose structure was confir