(S)-biphenyl-2-carboxylic acid [3-chloro-4-(3-hydroxymethyl-2,3,4,5-tetrahydrobenzo[e][1,4]diazepine-1-carbonyl)-phenyl]-amide

Base Information

Chemical Name:(S)-biphenyl-2-carboxylic acid [3-chloro-4-(3-hydroxymethyl-2,3,4,5-tetrahydrobenzo[e][1,4]diazepine-1-carbonyl)-phenyl]-amide
CAS No.:886225-49-6
Molecular Formula:C₃₀H₂₆ClN₃O₃
Molecular Weight:512.008
Hs Code.:

Synonyms:(S)-biphenyl-2-carboxylic acid [3-chloro-4-(3-hydroxymethyl-2,3,4,5-tetrahydrobenzo[e][1,4]diazepine-1-carbonyl)-phenyl]-amide

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Chemical Property of (S)-biphenyl-2-carboxylic acid [3-chloro-4-(3-hydroxymethyl-2,3,4,5-tetrahydrobenzo[e][1,4]diazepine-1-carbonyl)-phenyl]-amide

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Technology Process of (S)-biphenyl-2-carboxylic acid [3-chloro-4-(3-hydroxymethyl-2,3,4,5-tetrahydrobenzo[e][1,4]diazepine-1-carbonyl)-phenyl]-amide

There total 7 articles about (S)-biphenyl-2-carboxylic acid [3-chloro-4-(3-hydroxymethyl-2,3,4,5-tetrahydrobenzo[e][1,4]diazepine-1-carbonyl)-phenyl]-amide 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: 60.0%

: 1278520-74-3
(S)-tert-butyl 1-(4-biphenyl-2-ylcarboxamido-2-chlorobenzoyl)-3-(hydroxymethyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate

: 886225-49-6
(S)-biphenyl-2-carboxylic acid [3-chloro-4-(3-hydroxymethyl-2,3,4,5-tetrahydrobenzo[e][1,4]diazepine-1-carbonyl)-phenyl]-amide

Guidance literature:: (S)-tert-butyl 1-(4-biphenyl-2-ylcarboxamido-2-chlorobenzoyl)-3-(hydroxymethyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate; With hydrogenchloride; In 1,4-dioxane; at 20 ℃;

With water; sodium hydrogencarbonate; pH=7 - 8;

Reference yield:

: 200879-19-2
4-[([1,1'-biphenyl]-2-carbonyl)-amino]-2-chlorobenzoyl chloride

: 886225-47-4
(S)-tert-butyl 3-(hydroxymethyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate

: 886225-49-6
(S)-biphenyl-2-carboxylic acid [3-chloro-4-(3-hydroxymethyl-2,3,4,5-tetrahydrobenzo[e][1,4]diazepine-1-carbonyl)-phenyl]-amide

Guidance literature:: 4-[([1,1'-biphenyl]-2-carbonyl)-amino]-2-chlorobenzoyl chloride; (S)-tert-butyl 3-(hydroxymethyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate; With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 2.5h;

With hydrogenchloride; In dichloromethane; water; at 20 ℃; for 12h;

With ammonia; In dichloromethane; water; pH=8.5;

Reference yield:

: 947-84-2
2-Biphenylcarboxylic acid

: 886225-49-6
(S)-biphenyl-2-carboxylic acid [3-chloro-4-(3-hydroxymethyl-2,3,4,5-tetrahydrobenzo[e][1,4]diazepine-1-carbonyl)-phenyl]-amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / toluene / 5 - 20 °C

2.1: chloro-trimethyl-silane; pyridine / toluene / 0.5 h / 5 °C

2.2: 2.5 h / 5 °C

2.3: 35 - 85 °C

3.1: thionyl chloride / acetic acid butyl ester / 1.5 h / 64 °C

3.2: 20 °C / Cooling with ice

4.1: hydrogenchloride / 1,4-dioxane / 20 °C

4.2: pH 7 - 8

With pyridine; hydrogenchloride; chloro-trimethyl-silane; thionyl chloride; oxalyl dichloride; N,N-dimethyl-formamide; In 1,4-dioxane; acetic acid butyl ester; toluene;