[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl ester

Base Information

Chemical Name:[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl ester
CAS No.:428880-06-2
Molecular Formula:C₆₅H₉₈N₆O₇
Molecular Weight:1075.53
Hs Code.:

[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl ester

Synonyms:[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl ester

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Chemical Property of [6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl ester

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Technology Process of [6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl ester

There total 9 articles about [6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl 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: 67.0%

: 125376-03-6
3-(4-benzyloxy-phenyl)-2-butyrylamino-propionic acid 4-nitro-phenyl ester

: 851229-31-7
(3-aminopropyl)-[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]carbamic acid tert-butyl ester

: 428880-06-2
[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl ester

Guidance literature:: In methanol; at 20 ℃; for 1h;
DOI:10.1021/jm011067f

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 428880-06-2
[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / CHCl₃

2: 70 percent / H₂; 40percent aq. NaOH / Raney Ni / ethanol / 6 h / 20 °C / 775.74 Torr

3: 67 percent / methanol / 1 h / 20 °C

With hydrogen; nickel; In methanol; ethanol; chloroform;
DOI:10.1021/jm011067f

Reference yield:

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

: 428880-06-2
[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]{3-[2-butyrylamino-3-(4-benzyloxyphenyl)propionylamino]propyl}carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: ethyl chlorocarbonate; Et₃N / dioxane / 0.5 h

1.2: 70 percent / dioxane / 20 °C

2.1: 90 percent / 30percent HBr; AcOH; CF₃COOH / 2 h

3.1: 40 percent / 10 M BH₃*MeSMe / bis-(2-methoxy-ethyl) ether / 10 h / 120 °C

4.1: 35 percent / methanol / 3 h / 0 °C

5.1: 100 percent / CHCl₃

6.1: 70 percent / H₂; 40percent aq. NaOH / Raney Ni / ethanol / 6 h / 20 °C / 775.74 Torr

7.1: 67 percent / methanol / 1 h / 20 °C

With dimethylsulfide borane complex; hydrogen; chloroformic acid ethyl ester; acetic acid; triethylamine; trifluoroacetic acid; nickel; In 1,4-dioxane; methanol; ethanol; chloroform; diethylene glycol dimethyl ether;
DOI:10.1021/jm011067f