2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile

Base Information

Chemical Name:2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile
CAS No.:288629-16-3
Molecular Formula:C₃₈H₄₂N₂O₄
Molecular Weight:590.762
Hs Code.:

Synonyms:2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile

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Chemical Property of 2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile

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Technology Process of 2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile

There total 1 articles about 2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile 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: 66.0%

: 2627-86-3
(S)-1-phenyl-ethylamine

: 75-86-5
2-hydroxy-2-methylpropanenitrile

: 181629-23-2
2-(tri-O-benzyl-α-L-fucopyranosyl)-acetaldehyde

: 2(R)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile

: 288629-16-3
2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile

Guidance literature:: (S)-1-phenyl-ethylamine; 2-(tri-O-benzyl-α-L-fucopyranosyl)-acetaldehyde; With magnesium sulfate; In tetrahydrofuran; at 20 ℃;

2-hydroxy-2-methylpropanenitrile; In tetrahydrofuran; at -20 ℃;
DOI:10.1021/jo000034p

Reference yield: 81.0%

: 67-56-1
methanol

: 288629-16-3
2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile

: 288629-21-0
2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanoic acid methyl ester

Guidance literature:: With hydrogenchloride; at 0 ℃; for 2h;
DOI:10.1021/jo000034p

Reference yield:

: 288629-16-3
2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanenitrile

: 288629-19-6
2(S)-[(1(S)-phenylethyl)amino]-3-[2,3,4-tribenzyl-α-L-fucopyranosyl]propanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / hydrogen chloride / 2 h / 0 °C

2: 95 percent / lithium hydroxide / methanol; H₂O / 16 h / 20 °C / pH 9.5 - 10.5

With hydrogenchloride; lithium hydroxide; In methanol; water; 1: methanolysis / 2: Hydrolysis;
DOI:10.1021/jo000034p