(S)-2-Benzyloxycarbonylamino-4-[1-(benzyloxycarbonylmethyl-carbamoyl)-2-benzylsulfanyl-1-benzylsulfanylmethyl-ethylcarbamoyl]-butyric acid benzyl ester

Base Information

• Chemical Name: (S)-2-Benzyloxycarbonylamino-4-[1-(benzyloxycarbonylmethyl-carbamoyl)-2-benzylsulfanyl-1-benzylsulfanylmethyl-ethylcarbamoyl]-butyric acid benzyl ester
• CAS No.: 295788-11-3
• Molecular Formula: C₄₇H₄₉N₃O₈S₂
• Molecular Weight: 848.053
• Mol file: 295788-11-3.mol

Synonyms:(S)-2-Benzyloxycarbonylamino-4-[1-(benzyloxycarbonylmethyl-carbamoyl)-2-benzylsulfanyl-1-benzylsulfanylmethyl-ethylcarbamoyl]-butyric acid benzyl ester

Chemical Property of (S)-2-Benzyloxycarbonylamino-4-[1-(benzyloxycarbonylmethyl-carbamoyl)-2-benzylsulfanyl-1-benzylsulfanylmethyl-ethylcarbamoyl]-butyric acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-2-Benzyloxycarbonylamino-4-[1-(benzyloxycarbonylmethyl-carbamoyl)-2-benzylsulfanyl-1-benzylsulfanylmethyl-ethylcarbamoyl]-butyric acid benzyl ester

There total 5 articles about (S)-2-Benzyloxycarbonylamino-4-[1-(benzyloxycarbonylmethyl-carbamoyl)-2-benzylsulfanyl-1-benzylsulfanylmethyl-ethylcarbamoyl]-butyric 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: 60.0%

Cbz-(L)-Glu-OBn (3705-42-8) + (2-amino-3-benzylsulfanyl-2-benzylsulfanylmethyl-propionylamino)-acetic acid benzyl ester (295788-09-9) → (S)-2-Benzyloxycarbonylamino-4-[1-(benzyloxycarbonylmethyl-carbamoyl)-2-benzylsulfanyl-1-benzylsulfanylmethyl-ethylcarbamoyl]-butyric acid benzyl ester (295788-11-3)

Guidance literature:

With pyridine; dicyclohexyl-carbodiimide; In tetrahydrofuran; at 20 ℃; for 90h;

DOI:10.1016/S0960-894X(00)00281-X

Reference yield: 40.0%

glycine benzyl ester p-toluenesulfonic acid salt (1738-76-7) + (S)-2-Benzyloxycarbonylamino-5-(4,4-bis-benzylsulfanylmethyl-2,5-dioxo-oxazolidin-3-yl)-5-oxo-pentanoic acid benzyl ester (295788-10-2) → (S)-2-Benzyloxycarbonylamino-4-[1-(benzyloxycarbonylmethyl-carbamoyl)-2-benzylsulfanyl-1-benzylsulfanylmethyl-ethylcarbamoyl]-butyric acid benzyl ester (295788-11-3)

Guidance literature:

With 4-methyl-morpholine; TEA; In tetrahydrofuran; at 20 ℃; for 3h;

DOI:10.1016/S0960-894X(00)00281-X

Reference yield:

2,2-bis<(benzylthio)methyl>glycine (32418-96-5) → (S)-2-Benzyloxycarbonylamino-4-[1-(benzyloxycarbonylmethyl-carbamoyl)-2-benzylsulfanyl-1-benzylsulfanylmethyl-ethylcarbamoyl]-butyric acid benzyl ester (295788-11-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 86 percent / toluene; tetrahydrofuran / 1 h / 20 °C

2: DCC; pyridine / tetrahydrofuran / 24 h / 20 °C

3: 40 percent / TEA; NMM / tetrahydrofuran / 3 h / 20 °C

With 4-methyl-morpholine; pyridine; TEA; dicyclohexyl-carbodiimide; In tetrahydrofuran; toluene; 1: cyclocondensation / 2: Acylation / 3: Ring cleavage;

DOI:10.1016/S0960-894X(00)00281-X

upstream raw materials:

Cbz-(L)-Glu-OBn

(2-amino-3-benzylsulfanyl-2-benzylsulfanylmethyl-propionylamino)-acetic acid benzyl ester

glycine benzyl ester p-toluenesulfonic acid salt

(S)-2-Benzyloxycarbonylamino-5-(4,4-bis-benzylsulfanylmethyl-2,5-dioxo-oxazolidin-3-yl)-5-oxo-pentanoic acid benzyl ester