(2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-carboxy-2-isoxazolin-5-yl)propanoic acid

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Chemical Name:(2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-carboxy-2-isoxazolin-5-yl)propanoic acid
CAS No.:156426-53-8
Molecular Formula:C₁₅H₁₆N₂O₇
Molecular Weight:336.301
Hs Code.:

Synonyms:(2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-carboxy-2-isoxazolin-5-yl)propanoic acid

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Chemical Property of (2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-carboxy-2-isoxazolin-5-yl)propanoic acid

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Technology Process of (2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-carboxy-2-isoxazolin-5-yl)propanoic acid

There total 6 articles about (2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-carboxy-2-isoxazolin-5-yl)propanoic 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: 99.0%

: 156426-51-6
methyl (2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-(methoxycarbonyl)-2-isoxazolidin-5-yl)propanoate

: 156426-53-8
(2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-carboxy-2-isoxazolin-5-yl)propanoic acid

Guidance literature:: With sodium hydroxide; for 21h;
DOI:10.1021/ja00094a004

Reference yield: 90.0%

: C₁₈H₂₂N₂O₇

: 156426-53-8
(2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-carboxy-2-isoxazolin-5-yl)propanoic acid

Guidance literature:: With water; sodium hydroxide; In methanol;
DOI:10.1016/j.bmcl.2017.06.056

Reference yield:

: 16338-48-0
L-allylglycine

: 156426-53-8
(2S,5'R)-2-(N-(benzyloxycarbonyl)amino)-3-(3-carboxy-2-isoxazolin-5-yl)propanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / HCl

2: 45 percent / Et₃N, 4-(N,N-dimethylamino)pyridine / CHCl₃ / 19 h / 20 °C

3: 34 percent / aq. Na₂CO₃ / diethyl ether / 4 h / 20 °C

4: 99 percent / 10percent aq. NaOH / 21 h

With hydrogenchloride; dmap; sodium hydroxide; sodium carbonate; triethylamine; In diethyl ether; chloroform;
DOI:10.1021/ja00094a004