2-((E)-2-Benzyloxycarbonylamino-3-phenyl-acryloylamino)-acrylic acid methyl ester

Base Information

Chemical Name:2-((E)-2-Benzyloxycarbonylamino-3-phenyl-acryloylamino)-acrylic acid methyl ester
CAS No.:78464-47-8
Molecular Formula:C₂₁H₂₀N₂O₅
Molecular Weight:380.4
Hs Code.:

Synonyms:2-((E)-2-Benzyloxycarbonylamino-3-phenyl-acryloylamino)-acrylic acid methyl ester

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Chemical Property of 2-((E)-2-Benzyloxycarbonylamino-3-phenyl-acryloylamino)-acrylic acid methyl ester

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Technology Process of 2-((E)-2-Benzyloxycarbonylamino-3-phenyl-acryloylamino)-acrylic acid methyl ester

There total 2 articles about 2-((E)-2-Benzyloxycarbonylamino-3-phenyl-acryloylamino)-acrylic acid methyl ester 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: 86.0%

: 78464-22-9
2-((E)-2-Benzyloxycarbonylamino-3-phenyl-acryloylamino)-3-hydroxy-propionic acid methyl ester

: 78464-47-8
2-((E)-2-Benzyloxycarbonylamino-3-phenyl-acryloylamino)-acrylic acid methyl ester

Guidance literature:: With methanesulfonyl chloride; triethylamine; In dichloromethane; for 1.5h; Ambient temperature;
DOI:10.1246/bcsj.54.1132

Reference yield:

: 72015-61-3
(Z)-2-benzyloxycarbonylaminocinnamic acid

: 78464-47-8
2-((E)-2-Benzyloxycarbonylamino-3-phenyl-acryloylamino)-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / dicyclohexylcarbodiimide (DCC) / dimethylformamide / 12 h / Ambient temperature

2: 86 percent / mesyl chloride, triethylamine / CH₂Cl₂ / 1.5 h / Ambient temperature

With methanesulfonyl chloride; triethylamine; dicyclohexyl-carbodiimide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1246/bcsj.54.1132