{4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-carbamic acid tert-butyl ester
CAS No.:196704-57-1
Molecular Formula:C₅₈H₉₈N₆O₁₁
Molecular Weight:1055.45
Hs Code.:

{4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(<i>tert</i>-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-<i>tert</i>-butoxycarbonyl-amino)-propyl]-<i>tert</i>-butoxycarbonyl-amino}-propyl)-<i>tert</i>-butoxycarbonyl-amino]-butyl}-carbamic acid <i>tert</i>-butyl ester

Synonyms:{4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-carbamic acid tert-butyl ester

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Chemical Property of {4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-carbamic acid tert-butyl ester

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Technology Process of {4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-carbamic acid tert-butyl ester

There total 7 articles about {4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-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:

: {4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylideneamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-carbamic acid tert-butyl ester

: 196704-57-1
{4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-carbamic acid tert-butyl ester

Guidance literature:: With sodium tetrahydroborate; In ethanol; at 20 ℃; for 12h;
DOI:10.1016/S0040-4020(97)00801-6

Reference yield:

: 16652-64-5
O-benzyl-S-tyrosine

: 196704-57-1
{4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: 64 percent / SOCl₂ / 4 h / 40 °C

2.1: 67 percent / KF/Celite / acetonitrile / 10 h / Heating

3.1: 100 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

4.1: 94 percent / DIBAL / CH₂Cl₂; hexane / 1 h / 0 °C

5.1: oxalyl chloride; DMSO / CH₂Cl₂ / 0.67 h / -50 °C

5.2: 98 percent / Et₃N / CH₂Cl₂ / 0.17 h / -50 - 20 °C

6.1: Na₂SO₄ / ethanol / 24 h / 20 °C

7.1: 225.6 mg / NaBH₄ / ethanol / 12 h / 20 °C

With potassium fluoride; sodium tetrahydroborate; thionyl chloride; oxalyl dichloride; Celite; diisobutylaluminium hydride; dimethyl sulfoxide; sodium sulfate; triethylamine; In ethanol; hexane; dichloromethane; acetonitrile; 1.1: Esterification / 2.1: Alkylation / 3.1: Acylation / 4.1: Reduction / 5.1: Condensation / 5.2: Elimination / 6.1: Condensation / 7.1: Reduction;
DOI:10.1016/S0040-4020(97)00801-6

Reference yield:

: 57177-83-0
O-benzyltyrosine methyl ester

: 196704-57-1
{4-[(3-{[3-({3-[3-(4-benzyloxy-phenyl)-2-(tert-butoxycarbonyl-butyl-amino)-propylamino]-propyl}-tert-butoxycarbonyl-amino)-propyl]-tert-butoxycarbonyl-amino}-propyl)-tert-butoxycarbonyl-amino]-butyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 67 percent / KF/Celite / acetonitrile / 10 h / Heating

2.1: 100 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

3.1: 94 percent / DIBAL / CH₂Cl₂; hexane / 1 h / 0 °C

4.1: oxalyl chloride; DMSO / CH₂Cl₂ / 0.67 h / -50 °C

4.2: 98 percent / Et₃N / CH₂Cl₂ / 0.17 h / -50 - 20 °C

5.1: Na₂SO₄ / ethanol / 24 h / 20 °C

6.1: 225.6 mg / NaBH₄ / ethanol / 12 h / 20 °C

With potassium fluoride; sodium tetrahydroborate; oxalyl dichloride; Celite; diisobutylaluminium hydride; dimethyl sulfoxide; sodium sulfate; triethylamine; In ethanol; hexane; dichloromethane; acetonitrile; 1.1: Alkylation / 2.1: Acylation / 3.1: Reduction / 4.1: Condensation / 4.2: Elimination / 5.1: Condensation / 6.1: Reduction;
DOI:10.1016/S0040-4020(97)00801-6