8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide

Base Information

Chemical Name:8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide
CAS No.:109774-29-0
Molecular Formula:C₁₈H₁₄Cl₂N₄O
Molecular Weight:373.241
Hs Code.:

Synonyms:8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide

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Chemical Property of 8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide

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Technology Process of 8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide

There total 3 articles about 8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide 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: 83.0%

: 109774-52-9
8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carbonitrile

: 109774-29-0
8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide

Guidance literature:: With sulfuric acid; for 3h; Ambient temperature;
DOI:10.1002/jhet.5570230509

Reference yield: 73.0%

: 63176-94-3
8-chloro-6-(2-chlorophenyl)-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide

: 109774-29-0
8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide

Guidance literature:: With acetic acid; zinc; In dichloromethane; for 1h; Ambient temperature;
DOI:10.1002/jhet.5570230509

Reference yield:

: 109774-27-8
8-chloro-6-(2-chlorophenyl)-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carbonitrile

: 109774-29-0
8-chloro-6-(2-chlorophenyl)-5,6-dihydro-4H-imidazo<1,5-a><1,4>benzodiazepine-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / acetic acid, zinc dust / CH₂Cl₂ / 2 h / Ambient temperature

2: 83 percent / concentrated H₂SO₄ / 3 h / Ambient temperature

With sulfuric acid; acetic acid; zinc; In dichloromethane;
DOI:10.1002/jhet.5570230509