5-Chloro-3-nitro-2-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-benzoic acid methyl ester

Base Information

Chemical Name:5-Chloro-3-nitro-2-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-benzoic acid methyl ester
CAS No.:136285-63-7
Molecular Formula:C₄₆H₃₉ClN₆O₅
Molecular Weight:791.306
Hs Code.:

Synonyms:5-Chloro-3-nitro-2-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-benzoic acid methyl ester

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Chemical Property of 5-Chloro-3-nitro-2-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-benzoic acid methyl ester

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Technology Process of 5-Chloro-3-nitro-2-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-benzoic acid methyl ester

There total 4 articles about 5-Chloro-3-nitro-2-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-benzoic acid methyl 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: 32.0%

: 124750-51-2
N-(triephenylmethyl)-5-<4'-(bromomethyl)-biphenyl-2-yl>tetrazole

: 147330-24-3
methyl 5-chloro-3-nitro-2-valerylaminobenzoate

: 136285-63-7
5-Chloro-3-nitro-2-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-benzoic acid methyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; for 15h; Ambient temperature;
DOI:10.1021/jm00064a011

Reference yield:

: 5202-89-1
4-chlorobenzenesulfonyl chloride

: 136285-63-7
5-Chloro-3-nitro-2-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / triethylamine / CHCl₃ / 4 h / 0 °C

2: 60 percent / fuming nitric acid, acetic anhydride, conc. sulfuric acid / 4 h / Ambient temperature

3: 32 percent / K₂CO₃ / dimethylformamide / 15 h / Ambient temperature

With sulfuric acid; nitric acid; acetic anhydride; potassium carbonate; triethylamine; In chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm00064a011

Reference yield:

: 638-29-9
n-valeryl chloride

: 136285-63-7
5-Chloro-3-nitro-2-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / triethylamine / CHCl₃ / 4 h / 0 °C

2: 60 percent / fuming nitric acid, acetic anhydride, conc. sulfuric acid / 4 h / Ambient temperature

3: 32 percent / K₂CO₃ / dimethylformamide / 15 h / Ambient temperature

With sulfuric acid; nitric acid; acetic anhydride; potassium carbonate; triethylamine; In chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm00064a011