Thioacetic acid S-{(S)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} ester

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Chemical Name:Thioacetic acid S-{(S)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} ester
CAS No.:115370-33-7
Molecular Formula:C₂₃H₂₈N₂O₃S₂
Molecular Weight:444.619
Hs Code.:

Synonyms:Thioacetic acid S-{(S)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} ester

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Chemical Property of Thioacetic acid S-{(S)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} ester

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Technology Process of Thioacetic acid S-{(S)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} ester

There total 5 articles about Thioacetic acid S-{(S)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} 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: 26.0%

: 91702-98-6,80969-99-9
3-acetylthio-2-benzylpropanoic acid

: 84952-45-4
S-<(4-methylphenyl)methyl>-L-cysteinamide

: 115370-32-6
Thioacetic acid S-{(R)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} ester

: 115370-33-7
Thioacetic acid S-{(S)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} ester

Guidance literature:: With 4-methyl-morpholine; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In N,N-dimethyl-formamide; for 20h;
DOI:10.1021/jm00041a026

Reference yield:

: 5669-19-2
2-Benzyl-2-propenoic acid

: 115370-33-7
Thioacetic acid S-{(S)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} ester

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / CH₂Cl₂ / 1152 h

2: 7.6 percent / HOBT, EDC, N-methylmorpholine / dimethylformamide / 20 h

With 4-methyl-morpholine; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00041a026

Reference yield:

: 61925-77-7
Boc-cysteine(4-Me-Bn)

: 115370-33-7
Thioacetic acid S-{(S)-2-[(R)-1-carbamoyl-2-(4-methyl-benzylsulfanyl)-ethylcarbamoyl]-3-phenyl-propyl} ester

Guidance literature:: Multi-step reaction with 4 steps

1: Et₃N / tetrahydrofuran / 0.25 h / 0 - 5 °C

2: conc. NH₄OH / tetrahydrofuran / 18 h / Ambient temperature

3: 79 percent / CF₃COOH / CH₂Cl₂ / 44 h

4: 7.6 percent / HOBT, EDC, N-methylmorpholine / dimethylformamide / 20 h

With 4-methyl-morpholine; ammonium hydroxide; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00041a026