1261594-23-3

Basic information

• Product Name: 3-benzyl-7-chloro-1-methyl-3,4-dihydro-1H-benzo[d][1,3]diazepine-5(2H)-one
• Synonyms: 3-benzyl-7-chloro-1-methyl-3,4-dihydro-1H-benzo[d][1,3]diazepine-5(2H)-one
• CAS NO: 1261594-23-3
• Molecular Weight: 300.788
• Mol File: 1261594-23-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-benzyl-7-chloro-1-methyl-3,4-dihydro-1H-benzo[d][1,3]diazepine-5(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-benzyl-7-chloro-1-methyl-3,4-dihydro-1H-benzo[d][1,3]diazepine-5(2H)-one(1261594-23-3)
• EPA Substance Registry System: 3-benzyl-7-chloro-1-methyl-3,4-dihydro-1H-benzo[d][1,3]diazepine-5(2H)-one(1261594-23-3)

Safety Data

• Hazardous Substances Data: 1261594-23-3(Hazardous Substances Data)

Upstream product

• 93102-05-7 N-benzyl-N-(methoxymethyl)-N-[(trimethylsilyl)methyl]amine 
• 14529-12-5 6-chloro-N-methylisatoic anhydride 
• 4743-17-3 5-Chloroisatoic anhydride 

Relevant articles and documents

1,3-dipolar cycloaddition-decarboxylation reactions of an azomethine ylide with isatoic anhydrides: Formation of novel benzodiazepinones

A nonstabilized azomethine ylide reacts with a wide range of substituted isatoic anhydrides to afford novel 1,3-benzodiazepin-5-one derivatives, which are generally isolated in high yield. The transformations involve 1,3-dipolar cycloaddition reactions of the ylide with the anhydrides to give transient, and in a representative case spectroscopically observable, oxazolidine intermediates that undergo ring-opening-decarboxylation-ringclosing reaction cascades to yield the 1,3-benzodiazepin-5-one products.