(S)-[5-(4-acetyl-phenylcarbamoyl)-5-benzyloxycarbonylamino-pentyl]carbamic acid benzyl ester

Base Information

Chemical Name:(S)-[5-(4-acetyl-phenylcarbamoyl)-5-benzyloxycarbonylamino-pentyl]carbamic acid benzyl ester
CAS No.:1263384-52-6
Molecular Formula:C₃₀H₃₃N₃O₆
Molecular Weight:531.609
Hs Code.:

Synonyms:(S)-[5-(4-acetyl-phenylcarbamoyl)-5-benzyloxycarbonylamino-pentyl]carbamic acid benzyl ester

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Chemical Property of (S)-[5-(4-acetyl-phenylcarbamoyl)-5-benzyloxycarbonylamino-pentyl]carbamic acid benzyl ester

Chemical Property:

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Technology Process of (S)-[5-(4-acetyl-phenylcarbamoyl)-5-benzyloxycarbonylamino-pentyl]carbamic acid benzyl ester

There total 1 articles about (S)-[5-(4-acetyl-phenylcarbamoyl)-5-benzyloxycarbonylamino-pentyl]carbamic 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:

: 405-39-0
N,N'-di-[(phenylmethoxy)carbonyl]-L-lysine

: 99-92-3
p-aminobenzophenone

: 1263384-52-6
(S)-[5-(4-acetyl-phenylcarbamoyl)-5-benzyloxycarbonylamino-pentyl]carbamic acid benzyl ester

Guidance literature:: With 2,4,6-trimethyl-pyridine; HATU; In N,N-dimethyl-formamide; at 10 ℃; for 18h;

Reference yield:

: 1263384-52-6
(S)-[5-(4-acetyl-phenylcarbamoyl)-5-benzyloxycarbonylamino-pentyl]carbamic acid benzyl ester

: 1263384-53-7
(S)-{5-benzyloxycarbonylamino-5-[4-(2-bromo-acetyl)phenylcarbamoyl]pentyl}carbamic acid benzyl ester

Guidance literature:: With copper(ll) bromide; In chloroform; ethyl acetate; at 78 ℃; for 6h;

Reference yield:

: 1263384-52-6
(S)-[5-(4-acetyl-phenylcarbamoyl)-5-benzyloxycarbonylamino-pentyl]carbamic acid benzyl ester

: (S)-2,6-diamino-hexanoic acid [4-(2-{2-[4-(2-cyano-ethylamino)furazan-3-yl]benzoimidazol-1-yl}acetyl)phenyl]amide hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: copper(ll) bromide / ethyl acetate; chloroform / 6 h / 78 °C

2: potassium carbonate / N,N-dimethyl-formamide / 0.5 h / 20 °C

3: hydrogenchloride; hydrogen / palladium 10% on activated carbon / water; tetrahydrofuran; methanol / 5 h / 20 °C / 760.05 Torr

With hydrogenchloride; hydrogen; potassium carbonate; copper(ll) bromide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; chloroform; water; ethyl acetate; N,N-dimethyl-formamide;