(S)-2-{(S)-6-Benzyloxycarbonylamino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 4-benzyl ester 1-phenethyl ester

Base Information

Chemical Name:(S)-2-{(S)-6-Benzyloxycarbonylamino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 4-benzyl ester 1-phenethyl ester
CAS No.:161147-13-3
Molecular Formula:C₄₉H₅₇N₅O₁₀
Molecular Weight:876.019
Hs Code.:

(S)-2-{(S)-6-Benzyloxycarbonylamino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 4-benzyl ester 1-phenethyl ester

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Chemical Property of (S)-2-{(S)-6-Benzyloxycarbonylamino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 4-benzyl ester 1-phenethyl ester

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Technology Process of (S)-2-{(S)-6-Benzyloxycarbonylamino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 4-benzyl ester 1-phenethyl ester

There total 1 articles about (S)-2-{(S)-6-Benzyloxycarbonylamino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 4-benzyl ester 1-phenethyl 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:

: 3392-11-8
2,5-dioxopyrrolidin-1-yl N-(tert-butoxycarbonyl)-L-tryptophanate

: (S)-2-((S)-2-Amino-6-benzyloxycarbonylamino-hexanoylamino)-succinic acid 4-benzyl ester 1-phenethyl ester; compound with trifluoro-acetic acid

: 161147-13-3
(S)-2-{(S)-6-Benzyloxycarbonylamino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 4-benzyl ester 1-phenethyl ester

Guidance literature:: With benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; for 24h; Yield given; Ambient temperature;
DOI:10.1135/cccc19942511

Reference yield:

: 161147-13-3
(S)-2-{(S)-6-Benzyloxycarbonylamino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 4-benzyl ester 1-phenethyl ester

: (S)-2-{(S)-6-Amino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 1-phenethyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 6.5h; Ambient temperature;
DOI:10.1135/cccc19942511

Reference yield:

: 161147-13-3
(S)-2-{(S)-6-Benzyloxycarbonylamino-2-[(S)-2-tert-butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-succinic acid 4-benzyl ester 1-phenethyl ester

: (S)-2-[(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-6-(3-phenyl-ureido)-hexanoylamino]-succinic acid 1-phenethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd-C / methanol / 6.5 h / Ambient temperature

2: N-ethyldiisopropylamine / dimethylformamide / 20 h / Ambient temperature

With hydrogen; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; N,N-dimethyl-formamide;
DOI:10.1135/cccc19942511