220445-43-2

Upstream product

• 869309-08-0 7-chloro-2-hydroxy-9-(4-nitro-phenyl)-2,4-dihydro-1H-3,10,10a-triaza-benzo[f]azulene-2-carboxylic acid ethyl ester 
• 869309-07-9 8-chloro-1-(4-nitro-phenyl)-5H-benzo[d][1,2]diazepin-4-ylamine 
• 70-23-5 ethyl Bromopyruvate 
• 220444-98-4 8-chloro-1-(4-nitrophenyl)-3,5-dihydro-4H-2,3-benzodiazepin-4-thione 

Downstream Products

• 869309-11-5 9-(4-amino-phenyl)-7-chloro-4H-3,10,10a-triaza-benzo[f]azulene-2-carboxylic acid 
• 869309-13-7 [9-(4-amino-phenyl)-7-chloro-4H-3,10,10a-triaza-benzo[f]azulen-2-yl]-methanol 
• 869309-10-4 9-(4-amino-phenyl)-7-chloro-4H-3,10,10a-triaza-benzo[f]azulene-2-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

Potential metabolites of a condensed 2,3-benzodiazepine derivative

Putative metabolites of an AMPA antagonist imidazo-2,3-benzodiazepine (2) were synthesized and compared to constituents formed from the parent compound by a rat liver perfusion method. As metabolic transformations, hydroxylation of the 2-methyl group and