[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]-(2-cyanoethyl)carbamic acid tert-butyl ester

Base Information

Chemical Name:[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]-(2-cyanoethyl)carbamic acid tert-butyl ester
CAS No.:851228-45-0
Molecular Formula:C₄₅H₇₃N₅O₄
Molecular Weight:748.106
Hs Code.:

Synonyms:[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]-(2-cyanoethyl)carbamic acid tert-butyl ester

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Chemical Property of [6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]-(2-cyanoethyl)carbamic acid tert-butyl ester

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Technology Process of [6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]-(2-cyanoethyl)carbamic acid tert-butyl ester

There total 4 articles about [6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]-(2-cyanoethyl)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: 100.0%

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

: 428879-82-7
3-[6-({6-[(6-aminohexyl)benzylamino]hexyl}benzylamino)hexylamino]propionitrile

: 851228-45-0
[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]-(2-cyanoethyl)carbamic acid tert-butyl ester

Guidance literature:: In chloroform;
DOI:10.1021/jm011067f

Reference yield:

: 428879-80-5
6-aminohexanoic acid {6-[(6-aminohexanoyl)benzylamino]hexyl}benzylamide

: 851228-45-0
[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]-(2-cyanoethyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 40 percent / 10 M BH₃*MeSMe / bis-(2-methoxy-ethyl) ether / 10 h / 120 °C

2: 35 percent / methanol / 3 h / 0 °C

3: 100 percent / CHCl₃

With dimethylsulfide borane complex; In methanol; chloroform; diethylene glycol dimethyl ether;
DOI:10.1021/jm011067f

Reference yield:

: 428879-79-2
[5-(benzyl-{6-[benzyl-(6-benzyloxycarbonylaminohexanoyl)amino]hexyl}carbamoyl)pentyl]carbamic acid benzyl ester

: 851228-45-0
[6-(benzyl-{6-[benzyl-(6-tert-butoxycarbonylaminohexyl)amino]hexyl}amino)hexyl]-(2-cyanoethyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / 30percent HBr; AcOH; CF₃COOH / 2 h

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

3: 35 percent / methanol / 3 h / 0 °C

4: 100 percent / CHCl₃

With dimethylsulfide borane complex; acetic acid; trifluoroacetic acid; In methanol; chloroform; diethylene glycol dimethyl ether;
DOI:10.1021/jm011067f