{(S)-1-[1-[(S)-1-Cyclohexylmethyl-3-(dimethyl-phosphinoyl)-2-hydroxy-propylcarbamoyl]-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester

Base Information

• Chemical Name: {(S)-1-[1-[(S)-1-Cyclohexylmethyl-3-(dimethyl-phosphinoyl)-2-hydroxy-propylcarbamoyl]-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester
• CAS No.: 123381-45-3
• Molecular Formula: C₃₂H₅₀N₅O₆P
• Molecular Weight: 631.753
• Mol file: 123381-45-3.mol

Synonyms:

Chemical Property of {(S)-1-[1-[(S)-1-Cyclohexylmethyl-3-(dimethyl-phosphinoyl)-2-hydroxy-propylcarbamoyl]-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {(S)-1-[1-[(S)-1-Cyclohexylmethyl-3-(dimethyl-phosphinoyl)-2-hydroxy-propylcarbamoyl]-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester

There total 3 articles about {(S)-1-[1-[(S)-1-Cyclohexylmethyl-3-(dimethyl-phosphinoyl)-2-hydroxy-propylcarbamoyl]-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl 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:

N-tritylcyclohexylalaninol (123381-14-6) → {(S)-1-[1-[(S)-1-Cyclohexylmethyl-3-(dimethyl-phosphinoyl)-2-hydroxy-propylcarbamoyl]-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester (123381-45-3,123482-55-3,123482-63-3,123482-64-4)

Guidance literature:

Multi-step reaction with 4 steps

1: oxalyl chloride, dimethylsulfoxide, triethylamine / CH₂Cl₂ / 0.5 h / -60 °C

2: 1.) tert-butyllithium / 1.) THF, hexane, -78 deg C, 0.5 h, 2.) 0.5 h

3: 4.5 M HCl / dioxane / 0.5 h / Ambient temperature

4: 1-hydroxybenzotriazole monohydrate, N-methylmorpholine, 1-<3-(dimethylamino)propyl>-3-ethylcarbodiimide hydrochloride / dimethylformamide / 1.) -23 deg C, 2 h, 2.) room temp.

With 4-methyl-morpholine; hydrogenchloride; oxalyl dichloride; tert.-butyl lithium; dimethyl sulfoxide; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/jm00164a011

Reference yield:

N-tritylcyclohexylalaninal (112190-46-2) → {(S)-1-[1-[(S)-1-Cyclohexylmethyl-3-(dimethyl-phosphinoyl)-2-hydroxy-propylcarbamoyl]-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester (123381-45-3,123482-55-3,123482-63-3,123482-64-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 1.) tert-butyllithium / 1.) THF, hexane, -78 deg C, 0.5 h, 2.) 0.5 h

2: 4.5 M HCl / dioxane / 0.5 h / Ambient temperature

3: 1-hydroxybenzotriazole monohydrate, N-methylmorpholine, 1-<3-(dimethylamino)propyl>-3-ethylcarbodiimide hydrochloride / dimethylformamide / 1.) -23 deg C, 2 h, 2.) room temp.

With 4-methyl-morpholine; hydrogenchloride; tert.-butyl lithium; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; N,N-dimethyl-formamide;

DOI:10.1021/jm00164a011

Reference yield:

(S)-3-Amino-4-cyclohexyl-1-(dimethyl-phosphinoyl)-butan-2-ol; hydrochloride + N-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-L-histidine (63648-87-3) → {(S)-1-[1-[(S)-1-Cyclohexylmethyl-3-(dimethyl-phosphinoyl)-2-hydroxy-propylcarbamoyl]-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-2-phenyl-ethyl}-carbamic acid tert-butyl ester (123381-45-3,123482-55-3,123482-63-3,123482-64-4)

Guidance literature:

With 4-methyl-morpholine; 1-hydroxybenzotriazol-hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; 1.) -23 deg C, 2 h, 2.) room temp.;

DOI:10.1021/jm00164a011

upstream raw materials:

N-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-L-histidine

N-tritylcyclohexylalaninol

N-tritylcyclohexylalaninal