(5-{6-[6-(6-benzyloxycarbonylaminohexanoylamino)hexanoylamino]hexylcarbamoyl}pentyl)carbamic acid benzyl ester

Base Information

Chemical Name:(5-{6-[6-(6-benzyloxycarbonylaminohexanoylamino)hexanoylamino]hexylcarbamoyl}pentyl)carbamic acid benzyl ester
CAS No.:428879-75-8
Molecular Formula:C₄₀H₆₁N₅O₇
Molecular Weight:723.954
Hs Code.:

Synonyms:(5-{6-[6-(6-benzyloxycarbonylaminohexanoylamino)hexanoylamino]hexylcarbamoyl}pentyl)carbamic acid benzyl ester

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Chemical Property of (5-{6-[6-(6-benzyloxycarbonylaminohexanoylamino)hexanoylamino]hexylcarbamoyl}pentyl)carbamic acid benzyl ester

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Technology Process of (5-{6-[6-(6-benzyloxycarbonylaminohexanoylamino)hexanoylamino]hexylcarbamoyl}pentyl)carbamic acid benzyl ester

There total 4 articles about (5-{6-[6-(6-benzyloxycarbonylaminohexanoylamino)hexanoylamino]hexylcarbamoyl}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: 70.0%

: 26306-50-3
6-aminohexanoic acid (6-aminohexyl)amide

: 1947-00-8
6-(benzyloxycarbonylamino)hexanoic acid

: 428879-75-8
(5-{6-[6-(6-benzyloxycarbonylaminohexanoylamino)hexanoylamino]hexylcarbamoyl}pentyl)carbamic acid benzyl ester

Guidance literature:: 6-(benzyloxycarbonylamino)hexanoic acid; With chloroformic acid ethyl ester; triethylamine; In 1,4-dioxane; for 0.5h;

6-aminohexanoic acid (6-aminohexyl)amide; In 1,4-dioxane; at 20 ℃; Further stages.;
DOI:10.1021/jm011067f

Reference yield:

: 1947-00-8
6-(benzyloxycarbonylamino)hexanoic acid

: 428879-75-8
(5-{6-[6-(6-benzyloxycarbonylaminohexanoylamino)hexanoylamino]hexylcarbamoyl}pentyl)carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethyl chlorocarbonate; Et₃N / dioxane / 0.5 h

1.2: 78 percent / dioxane / 20 °C

2.1: 100 percent / H₂ / 10percent Pd/C / methanol / 2 h

3.1: ethyl chlorocarbonate; Et₃N / dioxane / 0.5 h

3.2: 70 percent / dioxane / 20 °C

With hydrogen; chloroformic acid ethyl ester; triethylamine; 10percent Pd/C; In 1,4-dioxane; methanol;
DOI:10.1021/jm011067f

Reference yield:

: 66095-18-9
N-benzyloxycarbonyl-1,6-hexanediamine

: 428879-75-8
(5-{6-[6-(6-benzyloxycarbonylaminohexanoylamino)hexanoylamino]hexylcarbamoyl}pentyl)carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethyl chlorocarbonate; Et₃N / dioxane / 0.5 h

1.2: 78 percent / dioxane / 20 °C

2.1: 100 percent / H₂ / 10percent Pd/C / methanol / 2 h

3.1: ethyl chlorocarbonate; Et₃N / dioxane / 0.5 h

3.2: 70 percent / dioxane / 20 °C

With hydrogen; chloroformic acid ethyl ester; triethylamine; 10percent Pd/C; In 1,4-dioxane; methanol;
DOI:10.1021/jm011067f