4-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-piperazine-1-carboxylic acid benzyl ester

Base Information

• Chemical Name: 4-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-piperazine-1-carboxylic acid benzyl ester
• CAS No.: 114457-63-5
• Molecular Formula: C₂₃H₂₇N₃O₅
• Molecular Weight: 425.484

Synonyms:4-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-piperazine-1-carboxylic acid benzyl ester

Chemical Property of 4-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-piperazine-1-carboxylic acid benzyl ester

Chemical Property:

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Technology Process of 4-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-piperazine-1-carboxylic acid benzyl ester

There total 2 articles about 4-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-piperazine-1-carboxylic acid benzyl 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:

phenylmethyl 1-piperazinecarboxylate (31166-44-6) + methyl (S)-2-isocyanato-3-phenylpropanoate (40203-94-9) → 4-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-piperazine-1-carboxylic acid benzyl ester (114457-63-5)

Guidance literature:

In dichloromethane; at 0 - 5 ℃; for 0.166667h;

DOI:10.1021/jm00120a006

Reference yield:

methyl (2S)-2-amino-3-phenylpropanoate hydrochloride (7524-50-7) → 4-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-piperazine-1-carboxylic acid benzyl ester (114457-63-5)

Guidance literature:

Multi-step reaction with 2 steps

1: toluene / 90 - 100 °C

2: CH₂Cl₂ / 0.17 h / 0 - 5 °C

In dichloromethane; toluene;

DOI:10.1021/jm00120a006

Reference yield:

4-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-piperazine-1-carboxylic acid benzyl ester (114457-63-5) → [(4-carbobenzyloxy-1-piperazinyl)carbonyl]-L-phenylalanine (114457-64-6)

Guidance literature:

With lithium hydroxide; In 1,4-dioxane; water; at 0 - 5 ℃; for 1h; Yield given;

DOI:10.1021/jm00120a006

upstream raw materials:

phenylmethyl 1-piperazinecarboxylate

methyl (S)-2-isocyanato-3-phenylpropanoate

methyl (2S)-2-amino-3-phenylpropanoate hydrochloride

Downstream raw materials:

[(4-carbobenzyloxy-1-piperazinyl)carbonyl]-L-phenylalanine

4-{(S)-1-[(S)-1-((1S,2R,3S)-1-Cyclohexylmethyl-2,3-dihydroxy-5-methyl-hexylcarbamoyl)-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethylcarbamoyl}-piperazine-1-carboxylic acid benzyl ester

(2S,3R,4S)-2-<<(1-piperazinylcarbonyl)-L-phenylalanyl-L-histidyl>amino>-1-cyclohexyl-3,4-dihydroxy-6-methylheptane bis(acetic acid) salt

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