(S)-N-(2-Oxo-tetrahydro-thiophen-3-yl)-2-(2-phenoxy-acetylamino)-3-phenyl-propionamide

Base Information

Chemical Name:(S)-N-(2-Oxo-tetrahydro-thiophen-3-yl)-2-(2-phenoxy-acetylamino)-3-phenyl-propionamide
CAS No.:1026560-20-2
Molecular Formula:C₂₁H₂₂N₂O₄S
Molecular Weight:398.483
Hs Code.:

Synonyms:(S)-N-(2-Oxo-tetrahydro-thiophen-3-yl)-2-(2-phenoxy-acetylamino)-3-phenyl-propionamide

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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)-N-(2-Oxo-tetrahydro-thiophen-3-yl)-2-(2-phenoxy-acetylamino)-3-phenyl-propionamide

Chemical Property:

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Technology Process of (S)-N-(2-Oxo-tetrahydro-thiophen-3-yl)-2-(2-phenoxy-acetylamino)-3-phenyl-propionamide

There total 3 articles about (S)-N-(2-Oxo-tetrahydro-thiophen-3-yl)-2-(2-phenoxy-acetylamino)-3-phenyl-propionamide 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:

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 1026560-20-2
(S)-N-(2-Oxo-tetrahydro-thiophen-3-yl)-2-(2-phenoxy-acetylamino)-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / 1-hydroxybenzotriazole, triethylamine, N-<3-(dimethylamino)propyl>-N'-ethylcarbodiimide hydrochloride / CH₂Cl₂ / 4 h / Ambient temperature

2: trifluoroacetic acid / CH₂Cl₂ / 4 h / Ambient temperature

3: 1-hydroxybenzotriazole, triethylamine, N-<3-(dimethylamino)propyl>-N'-ethylcarbodiimide hydrochloride / CH₂Cl₂ / 4 h / Ambient temperature

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/jm00052a002

Reference yield:

: 192310-93-3
[(S)-1-(2-Oxo-tetrahydro-thiophen-3-ylcarbamoyl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester

: 1026560-20-2
(S)-N-(2-Oxo-tetrahydro-thiophen-3-yl)-2-(2-phenoxy-acetylamino)-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / CH₂Cl₂ / 4 h / Ambient temperature

2: 1-hydroxybenzotriazole, triethylamine, N-<3-(dimethylamino)propyl>-N'-ethylcarbodiimide hydrochloride / CH₂Cl₂ / 4 h / Ambient temperature

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; In dichloromethane;
DOI:10.1021/jm00052a002

Reference yield:

: (S)-2-Amino-N-(2-oxo-tetrahydro-thiophen-3-yl)-3-phenyl-propionamide

: 122-59-8
2-phenoxyacetic acid

: 1026560-20-2
(S)-N-(2-Oxo-tetrahydro-thiophen-3-yl)-2-(2-phenoxy-acetylamino)-3-phenyl-propionamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; for 4h; Ambient temperature;
DOI:10.1021/jm00052a002