(2S,3S)-2-[2-((S)-2-Amino-3-tert-butoxy-propionylamino)-acetylamino]-3-methyl-pentanoic acid benzyl ester

Base Information

Chemical Name:(2S,3S)-2-[2-((S)-2-Amino-3-tert-butoxy-propionylamino)-acetylamino]-3-methyl-pentanoic acid benzyl ester
CAS No.:113727-12-1
Molecular Formula:C₂₂H₃₅N₃O₅
Molecular Weight:421.537
Hs Code.:

Synonyms:(2S,3S)-2-[2-((S)-2-Amino-3-tert-butoxy-propionylamino)-acetylamino]-3-methyl-pentanoic acid benzyl ester

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Chemical Property of (2S,3S)-2-[2-((S)-2-Amino-3-tert-butoxy-propionylamino)-acetylamino]-3-methyl-pentanoic acid benzyl ester

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Technology Process of (2S,3S)-2-[2-((S)-2-Amino-3-tert-butoxy-propionylamino)-acetylamino]-3-methyl-pentanoic acid benzyl ester

There total 4 articles about (2S,3S)-2-[2-((S)-2-Amino-3-tert-butoxy-propionylamino)-acetylamino]-3-methyl-pentanoic acid benzyl 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:

: 16652-75-8
L-isoleucine benzyl ester tosylate

: 113727-12-1
(2S,3S)-2-[2-((S)-2-Amino-3-tert-butoxy-propionylamino)-acetylamino]-3-methyl-pentanoic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / triethylamine, EEDQ / CH₂Cl₂ / 41 h

2: CF₃COOH / CH₂Cl₂ / 1 h / Ambient temperature

3: 89 percent / EEDQ / CH₂Cl₂ / 36 h / Ambient temperature

4: morpholine / 1 h / Ambient temperature

With morpholine; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; triethylamine; trifluoroacetic acid; In dichloromethane;

Reference yield:

: 113727-10-9
Glycyl-L-isoleucin-benzylester

: 113727-12-1
(2S,3S)-2-[2-((S)-2-Amino-3-tert-butoxy-propionylamino)-acetylamino]-3-methyl-pentanoic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / EEDQ / CH₂Cl₂ / 36 h / Ambient temperature

2: morpholine / 1 h / Ambient temperature

With morpholine; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In dichloromethane;

Reference yield:

: 90315-54-1
N-(tert-Butyloxycarbonyl)glycyl-L-isoleucin-benzylester

: 113727-12-1
(2S,3S)-2-[2-((S)-2-Amino-3-tert-butoxy-propionylamino)-acetylamino]-3-methyl-pentanoic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: CF₃COOH / CH₂Cl₂ / 1 h / Ambient temperature

2: 89 percent / EEDQ / CH₂Cl₂ / 36 h / Ambient temperature

3: morpholine / 1 h / Ambient temperature

With morpholine; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; trifluoroacetic acid; In dichloromethane;