(benzyloxycarbonyl)-β-tert-butyl-L-aspartyl-ψ(CH2-NH)-L-phenylalanine amide

Base Information

Chemical Name:(benzyloxycarbonyl)-β-tert-butyl-L-aspartyl-ψ(CH2-NH)-L-phenylalanine amide
CAS No.:98482-71-4
Molecular Formula:C₂₅H₃₃N₃O₅
Molecular Weight:455.554
Hs Code.:

Synonyms:(benzyloxycarbonyl)-β-tert-butyl-L-aspartyl-ψ(CH2-NH)-L-phenylalanine amide

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Chemical Property of (benzyloxycarbonyl)-β-tert-butyl-L-aspartyl-ψ(CH2-NH)-L-phenylalanine amide

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Technology Process of (benzyloxycarbonyl)-β-tert-butyl-L-aspartyl-ψ(CH2-NH)-L-phenylalanine amide

There total 3 articles about (benzyloxycarbonyl)-β-tert-butyl-L-aspartyl-ψ(CH2-NH)-L-phenylalanine amide 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: 60.0%

: 5241-58-7
L-Phenylalanine amide

: 98482-70-3
(S)-4-oxo-3-{[(phenylmethoxy)carbonyl]amino}butanoic acid 1,1-dimethylethyl ester

: 98482-71-4
(benzyloxycarbonyl)-β-tert-butyl-L-aspartyl-ψ(CH2-NH)-L-phenylalanine amide

Guidance literature:: With sodium cyanoborohydride; In methanol; acetic acid; for 3h;
DOI:10.1021/jm00150a020

Reference yield:

: 5545-52-8
Z-D(tBu)-OH

: 98482-71-4
(benzyloxycarbonyl)-β-tert-butyl-L-aspartyl-ψ(CH2-NH)-L-phenylalanine amide

Guidance literature:: Multi-step reaction with 3 steps

1: 78 percent / N,N'-dicyclohexylcarbodiimide (DCC), N,N-diisopropylethylamine (DIEA), 4-(dimethylamino)pyridine (DMAP) / CH₂Cl₂ / Ambient temperature

2: AlLiH₄ / tetrahydrofuran; diethyl ether / 1 h / 0 °C

3: 60 percent / sodium cyanoborohydride / methanol; acetic acid / 3 h

With dmap; lithium aluminium tetrahydride; sodium cyanoborohydride; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetic acid;
DOI:10.1021/jm00150a020

Reference yield:

: 98482-69-0
tert-butyl-(3S)-3-{[(benzyloxy)carbonyl]amino}-4-[methoxy(methyl)amino]-4-oxobutanoate

: 98482-71-4
(benzyloxycarbonyl)-β-tert-butyl-L-aspartyl-ψ(CH2-NH)-L-phenylalanine amide

Guidance literature:: Multi-step reaction with 2 steps

1: AlLiH₄ / tetrahydrofuran; diethyl ether / 1 h / 0 °C

2: 60 percent / sodium cyanoborohydride / methanol; acetic acid / 3 h

With lithium aluminium tetrahydride; sodium cyanoborohydride; In tetrahydrofuran; methanol; diethyl ether; acetic acid;
DOI:10.1021/jm00150a020