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N-(2-benzamido-1-carboxy-3-phenylpropyl)-Ala-Pro

Base Information Edit
  • Chemical Name:N-(2-benzamido-1-carboxy-3-phenylpropyl)-Ala-Pro
  • CAS No.:94730-83-3
  • Molecular Formula:C25H29N3O6
  • Molecular Weight:467.522
  • Hs Code.:
  • Mol file:94730-83-3.mol
N-(2-benzamido-1-carboxy-3-phenylpropyl)-Ala-Pro

Synonyms:N-(2-benzamido-1-carboxy-3-phenylpropyl)-Ala-Pro

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Chemical Property of N-(2-benzamido-1-carboxy-3-phenylpropyl)-Ala-Pro Edit
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Technology Process of N-(2-benzamido-1-carboxy-3-phenylpropyl)-Ala-Pro

There total 8 articles about N-(2-benzamido-1-carboxy-3-phenylpropyl)-Ala-Pro 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 7 steps
1: acetic acid / methanol / 72 h
2: 1.) HCl, 2.) di-tert-butyldicarbonate, triethylamine / 1.) RT, 24 h, 2.) methanol, 3 h
3: Amberlyst 15 resin / 240 h / 60 °C
4: triethylamine / CH2Cl2; methanol
5: TFA
6: triethylamine / CH2Cl2
7: 96 percent / aq. NaOH / 24 h
With hydrogenchloride; sodium hydroxide; Amberlyst 15 resin; di-tert-butyl dicarbonate; acetic acid; triethylamine; trifluoroacetic acid; In methanol; dichloromethane;
DOI:10.1021/jm00382a008
Guidance literature:
Multi-step reaction with 7 steps
1: acetic acid / methanol / 72 h
2: 1.) HCl, 2.) di-tert-butyldicarbonate, triethylamine / 1.) RT, 24 h, 2.) methanol, 3 h
3: Amberlyst 15 resin / 240 h / 60 °C
4: triethylamine / CH2Cl2; methanol
5: TFA
6: triethylamine / CH2Cl2
7: 96 percent / aq. NaOH / 24 h
With hydrogenchloride; sodium hydroxide; Amberlyst 15 resin; di-tert-butyl dicarbonate; acetic acid; triethylamine; trifluoroacetic acid; In methanol; dichloromethane;
DOI:10.1021/jm00382a008
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