[(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-hydroxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester

Base Information

• Chemical Name: [(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-hydroxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester
• CAS No.: 82537-92-6
• Molecular Formula: C₂₂H₂₉N₃O₆
• Molecular Weight: 431.489
• Mol file: 82537-92-6.mol

Synonyms:

Chemical Property of [(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-hydroxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-hydroxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester

There total 5 articles about [(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-hydroxymethyl-2-oxo-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:

[(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-benzyloxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester (81531-47-7) → [(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-hydroxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester (82537-92-6)

Guidance literature:

With hydrogen; palladium; In acetic acid; isopropyl alcohol; Ambient temperature;

Reference yield:

BOC-O-benzyl-L-serine (23680-31-1) → [(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-hydroxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester (82537-92-6)

Guidance literature:

Multi-step reaction with 3 steps

1: CH₃OK

2: 69.8 percent / CH₃OK / 2 h / 140 °C

3: 92 percent / H₂ / 10percent Pd/C / methanol

With potassium methanolate; hydrogen; palladium on activated charcoal; In methanol;

Reference yield:

N-carbobenzoxy-L-prolyl-L-phenylalanine methyl ester (23631-72-3) → [(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-hydroxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester (82537-92-6)

Guidance literature:

Multi-step reaction with 4 steps

1: H₂ / Pd / acetic acid

2: 110 °C

3: 1.) oxalyl chloride; 2.) N-methylmorpholine / 1.) CH₂Cl₂, -30 deg C, 15 min; 2.) -30 deg C, 30 min; RT, 12 h

4: H₂ / Pd / acetic acid; propan-2-ol / Ambient temperature

With 4-methyl-morpholine; oxalyl dichloride; hydrogen; palladium; In acetic acid; isopropyl alcohol;

upstream raw materials:

[(S)-2-((S)-3-Benzyl-1,4-dioxo-hexahydro-pyrrolo[1,2-a]pyrazin-2-yl)-1-benzyloxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester

BOC-O-benzyl-L-serine

N-carbobenzoxy-L-prolyl-L-phenylalanine methyl ester

(S)-proline-(S)-phenylalanine methyl ester