(S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid

Base Information

Chemical Name:(S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid
CAS No.:134675-10-8
Molecular Formula:C₃₅H₄₄N₆O₈
Molecular Weight:676.77
Hs Code.:

(S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid

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Chemical Property of (S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid

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Technology Process of (S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid

There total 6 articles about (S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid 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:

: 6404-28-0
Boc-Nle-OH

: 134675-10-8
(S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid

Guidance literature:: Multi-step reaction with 4 steps

1: N-methylmorpholine (NMM) / tetrahydrofuran / 0.1 h

2: N-methylmorpholine (NMM) / dimethylformamide

3: aq. HCl / acetic acid / 1.5 h

4: N,N-diisopropylethylamine (DIEA) / dimethylformamide / Ambient temperature

With 4-methyl-morpholine; hydrogenchloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00094a001

Reference yield:

: C₁₆H₂₉NO₆

: 134675-10-8
(S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid

Guidance literature:: Multi-step reaction with 3 steps

1: N-methylmorpholine (NMM) / dimethylformamide

2: aq. HCl / acetic acid / 1.5 h

3: N,N-diisopropylethylamine (DIEA) / dimethylformamide / Ambient temperature

With 4-methyl-morpholine; hydrogenchloride; N-ethyl-N,N-diisopropylamine; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00094a001

Reference yield:

: 783280-20-6
(S)-3-Amino-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid

: 134675-10-8
(S)-3-{(S)-2-[(S)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionylamino]-hexanoylamino}-N-((E)-1-carbamoyl-2-phenyl-vinyl)-succinamic acid

Guidance literature:: Multi-step reaction with 3 steps

1: N-methylmorpholine (NMM) / dimethylformamide

2: aq. HCl / acetic acid / 1.5 h

3: N,N-diisopropylethylamine (DIEA) / dimethylformamide / Ambient temperature

With 4-methyl-morpholine; hydrogenchloride; N-ethyl-N,N-diisopropylamine; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00094a001