4-[3-(4-Chloro-phenyl)-ureido]-4-dipentylcarbamoyl-butyric acid benzyl ester

Base Information

Chemical Name:4-[3-(4-Chloro-phenyl)-ureido]-4-dipentylcarbamoyl-butyric acid benzyl ester
CAS No.:117997-61-2
Molecular Formula:C₂₉H₄₀ClN₃O₄
Molecular Weight:530.107
Hs Code.:

Synonyms:4-[3-(4-Chloro-phenyl)-ureido]-4-dipentylcarbamoyl-butyric acid benzyl ester

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Chemical Property of 4-[3-(4-Chloro-phenyl)-ureido]-4-dipentylcarbamoyl-butyric acid benzyl ester

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Technology Process of 4-[3-(4-Chloro-phenyl)-ureido]-4-dipentylcarbamoyl-butyric acid benzyl ester

There total 4 articles about 4-[3-(4-Chloro-phenyl)-ureido]-4-dipentylcarbamoyl-butyric acid benzyl 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: 84.0%

: 118100-27-9
ε-benzyl-DL-glutamic acid dipentylamide hydrochloride

: 104-12-1
p-chlorphenylisocyanate

: 117997-61-2
4-[3-(4-Chloro-phenyl)-ureido]-4-dipentylcarbamoyl-butyric acid benzyl ester

Guidance literature:: With triethylamine; In tetrahydrofuran; for 24h; Ambient temperature;
DOI:10.1021/jm00164a020

Reference yield:

: 117997-81-6
5-(benzyloxy)-2-(tert-butoxycarbonylamino)-5-oxopentanoic acid

: 117997-61-2
4-[3-(4-Chloro-phenyl)-ureido]-4-dipentylcarbamoyl-butyric acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 48 percent / 1-<3-(dimethylamino)propyl>-3-ethylcarbodiimide hydrochloride / CH₂Cl₂ / pH >8.5

2: 75 percent / HCl gas / ethyl acetate / 0.33 h / -25 °C

3: 84 percent / Et₃N / tetrahydrofuran / 24 h / Ambient temperature

With hydrogenchloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1021/jm00164a020

Reference yield:

: 118100-26-8
N^α-Boc-ε-benzyl-DL-glutamic acid dipentylamide

: 117997-61-2
4-[3-(4-Chloro-phenyl)-ureido]-4-dipentylcarbamoyl-butyric acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / HCl gas / ethyl acetate / 0.33 h / -25 °C

2: 84 percent / Et₃N / tetrahydrofuran / 24 h / Ambient temperature

With hydrogenchloride; triethylamine; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/jm00164a020