2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxyphenyl)propyl ester

Base Information

Chemical Name:2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxyphenyl)propyl ester
CAS No.:1370339-76-6
Molecular Formula:C₆₄H₅₇ClN₆O₄
Molecular Weight:1009.65
Hs Code.:

Synonyms:2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxyphenyl)propyl ester

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Chemical Property of 2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxyphenyl)propyl ester

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Technology Process of 2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxyphenyl)propyl ester

There total 6 articles about 2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxyphenyl)propyl ester 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: 25.0%

: 1370339-75-5
2-n-butyl-5-chloro-3H-imidazole-4-carboxylic acid 3-(3,4-bisbenzyloxyphenyl)propyl ester

: 133051-88-4
N-(triphenylmethyl)-5-<4'-(bromomethyl)biphenyl-2-yl>tetrazole

: 1370339-77-7
2-n-butyl-5-chloro-1-[2'-(2-trityl-2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxy-phenyl)propyl ester

: 1370339-76-6
2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxyphenyl)propyl ester

Guidance literature:: With tetrabutyl phosphonium bromide; sodium hydroxide; In dichloromethane; water; at 20 ℃; for 24h;
DOI:10.1016/j.ejmech.2012.01.043

Reference yield:

: 1078-61-1
dihydrocaffeic acid

: 1370339-76-6
2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxyphenyl)propyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 20 h / 60 °C / Inert atmosphere

2.1: lithium aluminium tetrahydride / tetrahydrofuran; diethyl ether / 2.5 h / 0 - 20 °C

2.2: pH 1

3.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran; diethyl ether / 12 h / 20 °C

4.1: tetrabutyl phosphonium bromide; sodium hydroxide / dichloromethane; water / 24 h / 20 °C

With lithium aluminium tetrahydride; tetrabutyl phosphonium bromide; potassium carbonate; triphenylphosphine; sodium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; diethyl ether; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.01.043

Reference yield:

: 524004-38-4
3-[3,4-bis(benzyloxy)phenyl]propan-1-ol

: 1370339-76-6
2-n-butyl-5-chloro-3-[2'-(2-trityl-2H-tetrazol-5-yl)biphenyl-4-ylmethyl]-3H-imidazole-4-carboxylic acid 3-(3,4-bis-benzyloxyphenyl)propyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran; diethyl ether / 12 h / 20 °C

2: tetrabutyl phosphonium bromide; sodium hydroxide / dichloromethane; water / 24 h / 20 °C

With tetrabutyl phosphonium bromide; triphenylphosphine; sodium hydroxide; diethylazodicarboxylate; In tetrahydrofuran; diethyl ether; dichloromethane; water;
DOI:10.1016/j.ejmech.2012.01.043