8-bromo-1-(2-phthalimidoethyl)-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine

Base Information

Chemical Name:8-bromo-1-(2-phthalimidoethyl)-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine
CAS No.:60640-15-5
Molecular Formula:C₂₆H₁₈BrN₅O₂
Molecular Weight:512.365
Hs Code.:

Synonyms:8-bromo-1-(2-phthalimidoethyl)-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine

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Chemical Property of 8-bromo-1-(2-phthalimidoethyl)-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine

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Technology Process of 8-bromo-1-(2-phthalimidoethyl)-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine

There total 5 articles about 8-bromo-1-(2-phthalimidoethyl)-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propionic acid N'-(7-bromo-5-phenyl-3H-benzo[e][1,4]diazepin-2-yl)-hydrazide

: 60640-15-5
8-bromo-1-(2-phthalimidoethyl)-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine

Guidance literature:: In acetic acid; at 117 ℃; for 0.7h; Yield given;
DOI:10.1021/jm00178a009

Reference yield:

: 3339-73-9
3-phthalimidopropanoic acid

: 60640-15-5
8-bromo-1-(2-phthalimidoethyl)-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) carbonyldiimidazole / 1.) THF, RT, 72 min, 2.) THF, RT, 18 h

2: acetic acid / 0.7 h / 117 °C

With 1,1'-carbonyldiimidazole; In acetic acid;
DOI:10.1021/jm00178a009

Reference yield:

: 72874-57-8
7-bromo-2-hydrazino-5-phenyl-3H-[1,4]benzodiazepine

: 60640-15-5
8-bromo-1-(2-phthalimidoethyl)-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepine

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) carbonyldiimidazole / 1.) THF, RT, 72 min, 2.) THF, RT, 18 h

2: acetic acid / 0.7 h / 117 °C

With 1,1'-carbonyldiimidazole; In acetic acid;
DOI:10.1021/jm00178a009