(S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Base Information

• Chemical Name: (S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
• CAS No.: 123984-01-0
• Molecular Formula: C₂₂H₃₂N₄O₆
• Molecular Weight: 448.519
• Mol file: 123984-01-0.mol

Synonyms:(S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Chemical Property of (S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

There total 4 articles about (S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic 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: 90.0%

(S)-2-[(S)-1-((S)-1-Benzyloxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (123984-23-6) → (S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (123984-01-0)

Guidance literature:

With hydrogen; palladium on activated charcoal; In methanol; for 1h; Ambient temperature;

DOI:10.1248/cpb.38.1007

Reference yield:

1-(tert-butoxycarbonyl)-L-proline (15761-39-4,59433-50-0) → (S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (123984-01-0)

Guidance literature:

Multi-step reaction with 2 steps

1: triethylamine (TEA), dicyclohexylcarbodiimide (DCC), N-hydroxybenzotriazole (HOBt) / dimethylformamide; CH₂Cl₂ / 5 °C

2: 90 percent / H₂ / 5percent Pd-C / methanol / 1 h / Ambient temperature

With hydrogen; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1248/cpb.38.1007

Reference yield:

[(S)-1-((S)-1-Benzyloxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester (123984-22-5) → (S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (123984-01-0)

Guidance literature:

Multi-step reaction with 3 steps

1: HCl / ethyl acetate / Ambient temperature

2: triethylamine (TEA), dicyclohexylcarbodiimide (DCC), N-hydroxybenzotriazole (HOBt) / dimethylformamide; CH₂Cl₂ / 5 °C

3: 90 percent / H₂ / 5percent Pd-C / methanol / 1 h / Ambient temperature

With hydrogenchloride; hydrogen; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; palladium on activated charcoal; In methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;

DOI:10.1248/cpb.38.1007

upstream raw materials:

(S)-2-[(S)-1-((S)-1-Benzyloxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

1-(tert-butoxycarbonyl)-L-proline

[(S)-1-((S)-1-Benzyloxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester

Downstream raw materials:

(S)-2-[(S)-1-((S)-1-Hydroxycarbamoyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid benzyl ester