(S)-5-chloro-2-(4-chlorophenylcarbamoyl)phenyl 2-(benzyloxycarbonylamino)propanoate

Base Information

Chemical Name:(S)-5-chloro-2-(4-chlorophenylcarbamoyl)phenyl 2-(benzyloxycarbonylamino)propanoate
CAS No.:1169776-78-6
Molecular Formula:C₂₄H₂₀Cl₂N₂O₅
Molecular Weight:487.339
Hs Code.:

Synonyms:(S)-5-chloro-2-(4-chlorophenylcarbamoyl)phenyl 2-(benzyloxycarbonylamino)propanoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-5-chloro-2-(4-chlorophenylcarbamoyl)phenyl 2-(benzyloxycarbonylamino)propanoate

Chemical Property:

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Technology Process of (S)-5-chloro-2-(4-chlorophenylcarbamoyl)phenyl 2-(benzyloxycarbonylamino)propanoate

There total 1 articles about (S)-5-chloro-2-(4-chlorophenylcarbamoyl)phenyl 2-(benzyloxycarbonylamino)propanoate 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: 57.0%

: 1142-20-7
N-Cbz-Ala

: 106628-82-4
4-chloro-N-(4-chloro-phenyl)-2-hydroxy-benzamide

: 1169776-78-6
(S)-5-chloro-2-(4-chlorophenylcarbamoyl)phenyl 2-(benzyloxycarbonylamino)propanoate

Guidance literature:: With dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at -10 - 4 ℃; for 24h;
DOI:10.1016/j.bmc.2009.04.008

Reference yield:

: 1169776-78-6
(S)-5-chloro-2-(4-chlorophenylcarbamoyl)phenyl 2-(benzyloxycarbonylamino)propanoate

: 1227476-86-9
BrH*C₁₆H₁₄Cl₂N₂O₃

Guidance literature:: With hydrogen bromide; In acetic acid;
DOI:10.3390/molecules16032414

Reference yield:

: 1169776-78-6
(S)-5-chloro-2-(4-chlorophenylcarbamoyl)phenyl 2-(benzyloxycarbonylamino)propanoate

: 1227477-25-9
C₁₆H₁₄Cl₂N₂O₃

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen bromide / acetic acid

2: triethylamine / chloroform

With hydrogen bromide; triethylamine; In chloroform; acetic acid;
DOI:10.3390/molecules16032414