36985-45-2

Upstream product

• 124-40-3 dimethyl amine 
• 22316-55-8 N-desmethylclobazam 
• 62-53-3 aniline 
• 700-37-8 4-chloro-2-fluoro-nitrobenzene 
• 25781-92-4 5-chloro-2-nitro-N-phenylaniline 
• 68406-47-3 4-chloro-N₂-phenylbenzene-1,2-diamine 

Downstream Products

• 54748-06-0 8-chloro-1-methyl-6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,5>benzodiazepin-5(6H)-one 
• 54705-80-5 8-chloro-6-phenyl-4H-<1,24>triazolo<4,3-a><1,5>benzodiazepin-5(6H)-one 
• 153901-40-7 6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,5>benzodiazepine-5(6H)-thione 
• 153901-44-1 8-Chloro-5-methylsulfanyl-6-phenyl-6H-2,3,6,10b-tetraaza-benzo[e]azulene 
• 153901-41-8 8-chloro-1-methyl-6-phenyl-4H-<1,2,4>triazolo<4,3-a><1,5>benzodiazepine-5(6H)-thione 
• 153901-45-2 8-Chloro-1-methyl-5-methylsulfanyl-6-phenyl-6H-2,3,6,10b-tetraaza-benzo[e]azulene 
• 153901-51-0 (8-Chloro-6-phenyl-6H-2,3,6,10b-tetraaza-benzo[e]azulen-5-yl)-dimethyl-amine 
• 153901-42-9 8-chloro-1,6-diphenyl-4H-<1,2,4>triazolo<4,3-a><1,5>benzodiazepine-5(6H)-thione 
• 153901-47-4 [2-(8-Chloro-6-phenyl-6H-2,3,6,10b-tetraaza-benzo[e]azulen-5-ylsulfanyl)-ethyl]-dimethyl-amine 
• 153901-52-1 8-Chloro-5-morpholin-4-yl-6-phenyl-6H-2,3,6,10b-tetraaza-benzo[e]azulene 
• 153901-46-3 8-Chloro-5-methylsulfanyl-1,6-diphenyl-6H-2,3,6,10b-tetraaza-benzo[e]azulene 
• 153901-57-6 (8-Chloro-1,6-diphenyl-6H-2,3,6,10b-tetraaza-benzo[e]azulen-5-yl)-dimethyl-amine 
• 153901-55-4 8-Chloro-1-methyl-5-morpholin-4-yl-6-phenyl-6H-2,3,6,10b-tetraaza-benzo[e]azulene 
• 153901-48-5 RL 236 

Relevant academic research and scientific papers

DERIVATIVES OF 1-PHENYL-1,5-DIHYDRO-BENZO[B] [1.4]DIAZEPINE-2.4-DIONE AS INHIBITORS OF HIV REPLICATION

Compounds of formula (I) wherein m, R1, R2, R3, X and Y are defined herein, are useful as inhibitors of HIV replication.

1,5-Benzodiazepines XI. 5-(Dialkylamino) or 5-(alkylthio) substituted 8-chloro-6-phenyl-6H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepines with anticonvulsant activity

The cyclocondensation of (dimethylamino)benzodiazepinones 3a,b with hydrazides yielded triazolobenzodiazepinones 4 which were treated with Lawesson's reagent to give thiolactams 5. The phase-transfer catalyzed (TEBA) alkylation of compounds 5 with suitabl

2-Amino-5-phenyl-4H-3,5-dihydro-1,5-benzodiazepin-4-ones and salts thereof

Compounds of the formula SPC1 Wherein R1 and R2 are each hydrogen or methyl, and R3 is chlorine, bromine or nitro, and non-toxic, pharmacologically acceptable acid addition salts thereof; the compounds as well as their sal