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(2S)-2-((3S)-3-{[(benzyloxy)carbonyl]amino}-2-oxopyrrolidin-1-yl)propanoic acid

Base Information
  • Chemical Name:(2S)-2-((3S)-3-{[(benzyloxy)carbonyl]amino}-2-oxopyrrolidin-1-yl)propanoic acid
  • CAS No.:217969-71-6
  • Molecular Formula:C15H18N2O5
  • Molecular Weight:306.318
  • Hs Code.:
(2S)-2-((3S)-3-{[(benzyloxy)carbonyl]amino}-2-oxopyrrolidin-1-yl)propanoic acid

Synonyms:(2S)-2-((3S)-3-{[(benzyloxy)carbonyl]amino}-2-oxopyrrolidin-1-yl)propanoic acid

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Chemical Property of (2S)-2-((3S)-3-{[(benzyloxy)carbonyl]amino}-2-oxopyrrolidin-1-yl)propanoic acid
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Technology Process of (2S)-2-((3S)-3-{[(benzyloxy)carbonyl]amino}-2-oxopyrrolidin-1-yl)propanoic acid

There total 3 articles about (2S)-2-((3S)-3-{[(benzyloxy)carbonyl]amino}-2-oxopyrrolidin-1-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:
Guidance literature:
Multi-step reaction with 2 steps
1.1: MeI / acetone / 72 h / 20 °C
1.2: 28 percent / Dowex resin (hydroxide form) / acetonitrile / 18 h / 20 °C
2.1: 99.9 percent / TFA / CH2Cl2 / 4 h / 20 °C
With trifluoroacetic acid; methyl iodide; In dichloromethane; acetone;
DOI:10.1021/jm060870c
Guidance literature:
Multi-step reaction with 3 steps
1.1: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; N-hydroxybenzotriazole; Et3N / dimethylformamide / 1 h
1.2: 82 percent / dimethylformamide / 18 h
2.1: MeI / acetone / 72 h / 20 °C
2.2: 28 percent / Dowex resin (hydroxide form) / acetonitrile / 18 h / 20 °C
3.1: 99.9 percent / TFA / CH2Cl2 / 4 h / 20 °C
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; methyl iodide; In dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm060870c
Guidance literature:
Multi-step reaction with 2 steps
1: DOWEX [OH](-) / acetonitrile
2: TFA / CH2Cl2 / 20 °C
With DOWEX [OH](-); trifluoroacetic acid; In dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2006.04.053
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