[5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-tert-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-tert-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-carbamic acid tert-butyl ester
CAS No.:289889-17-4
Molecular Formula:C₇₅H₁₁₂N₆O₁₁
Molecular Weight:1273.75
Hs Code.:

[5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-<i>tert</i>-butoxycarbonyl-amino)-hexyl]-<i>tert</i>-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-<i>tert</i>-butoxycarbonyl-amino)-hexyl]-carbamic acid <i>tert</i>-butyl ester

Synonyms:[5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-tert-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-carbamic acid tert-butyl ester

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Chemical Property of [5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-tert-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-carbamic acid tert-butyl ester

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Technology Process of [5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-tert-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-carbamic acid tert-butyl ester

There total 11 articles about [5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-tert-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-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:

: 1,3-bis-benzylamino-propan-2-one

: 213772-98-6
N-(N'-benzyl-N'-tert-butoxycarbonyl-6-aminohexyl)-N-tert-butoxycarbonyl-6-aminohexanoic acid

: 289889-17-4
[5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-tert-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-carbamic acid tert-butyl ester

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/S0968-0896(00)00055-9

Reference yield:

: 4048-33-3
6-amino-1-hexanol

: 289889-17-4
[5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-tert-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: K₂CO₃ / acetonitrile / 120 h / 20 °C

2: CH₂Cl₂ / 2 h / 0 °C

3: 69 percent / PDC / dimethylformamide / 20 °C

4: BOP; Et₃N / CH₂Cl₂ / 2 h / 20 °C

With dipyridinium dichromate; potassium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1: Substitution / 2: Substitution / 3: Oxidation / 4: Acylation;
DOI:10.1016/S0968-0896(00)00055-9

Reference yield:

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

: 289889-17-4
[5-(benzyl-{3-[benzyl-(6-{[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-tert-butoxycarbonyl-amino}-hexanoyl)-amino]-2-oxo-propyl}-carbamoyl)-pentyl]-[6-(benzyl-tert-butoxycarbonyl-amino)-hexyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: CH₂Cl₂ / 3 h / 0 °C

2: 53 percent / Et₃N / diethyl ether / 3 h / 20 °C

3: K₂CO₃ / acetonitrile / 120 h / 20 °C

4: CH₂Cl₂ / 2 h / 0 °C

5: 69 percent / PDC / dimethylformamide / 20 °C

6: BOP; Et₃N / CH₂Cl₂ / 2 h / 20 °C

With dipyridinium dichromate; potassium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 1: Substitution / 2: Tosylation / 3: Substitution / 4: Substitution / 5: Oxidation / 6: Acylation;
DOI:10.1016/S0968-0896(00)00055-9