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(S)-1-[(R)-2-(2-Amino-acetylamino)-2-methyl-butyryl]-pyrrolidine-2-carboxylic acid [(4-nitro-phenylcarbamoyl)-methyl]-amide

Base Information Edit
  • Chemical Name:(S)-1-[(R)-2-(2-Amino-acetylamino)-2-methyl-butyryl]-pyrrolidine-2-carboxylic acid [(4-nitro-phenylcarbamoyl)-methyl]-amide
  • CAS No.:1026446-76-3
  • Molecular Formula:C20H28N6O6
  • Molecular Weight:448.479
  • Hs Code.:
  • Mol file:1026446-76-3.mol
(S)-1-[(R)-2-(2-Amino-acetylamino)-2-methyl-butyryl]-pyrrolidine-2-carboxylic acid [(4-nitro-phenylcarbamoyl)-methyl]-amide

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Chemical Property of (S)-1-[(R)-2-(2-Amino-acetylamino)-2-methyl-butyryl]-pyrrolidine-2-carboxylic acid [(4-nitro-phenylcarbamoyl)-methyl]-amide Edit
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Technology Process of (S)-1-[(R)-2-(2-Amino-acetylamino)-2-methyl-butyryl]-pyrrolidine-2-carboxylic acid [(4-nitro-phenylcarbamoyl)-methyl]-amide

There total 3 articles about (S)-1-[(R)-2-(2-Amino-acetylamino)-2-methyl-butyryl]-pyrrolidine-2-carboxylic acid [(4-nitro-phenylcarbamoyl)-methyl]-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:
Guidance literature:
Multi-step reaction with 4 steps
1: 82 percent / DCC, HOBt
2: 88 percent / NaOH / methanol / 2 h / Ambient temperature
3: 1.) TFA, 2.) DCC, HOBt / 1.) room temperature, 30 min, 2.) CH2Cl2, room temperature, overnight
4: TFA / 0.33 h / Ambient temperature
With sodium hydroxide; benzotriazol-1-ol; dicyclohexyl-carbodiimide; trifluoroacetic acid; In methanol;
DOI:10.1039/P19950002115
Guidance literature:
Multi-step reaction with 3 steps
1: 88 percent / NaOH / methanol / 2 h / Ambient temperature
2: 1.) TFA, 2.) DCC, HOBt / 1.) room temperature, 30 min, 2.) CH2Cl2, room temperature, overnight
3: TFA / 0.33 h / Ambient temperature
With sodium hydroxide; benzotriazol-1-ol; dicyclohexyl-carbodiimide; trifluoroacetic acid; In methanol;
DOI:10.1039/P19950002115
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) TFA, 2.) DCC, HOBt / 1.) room temperature, 30 min, 2.) CH2Cl2, room temperature, overnight
2: TFA / 0.33 h / Ambient temperature
With benzotriazol-1-ol; dicyclohexyl-carbodiimide; trifluoroacetic acid;
DOI:10.1039/P19950002115
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