benzyl (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionate

Base Information

• Chemical Name: benzyl (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionate
• CAS No.: 127944-63-2
• Molecular Formula: C₂₃H₂₉NO₅
• Molecular Weight: 399.487
• Mol file: 127944-63-2.mol

Synonyms:benzyl (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionate

Chemical Property of benzyl (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of benzyl (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionate

There total 2 articles about benzyl (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionate 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:

2-<<(benzyloxy)carbonyl>methylamino>-1-(methoxymethoxy)ethane (122225-41-6) → benzyl (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionate (127944-63-2)

Guidance literature:

Multi-step reaction with 2 steps

1: 84 percent / H₂ / 10percent Pd/C / methanol / 12 h

2: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) CH₂Cl₂, -10 deg C, 3 min, 2a.) -10 deg, 15 min, 2b.) RT, 2 h

With 4-methyl-morpholine; hydrogen; isobutyl chloroformate; palladium on activated charcoal; In methanol;

DOI:10.1021/jm00169a024

Reference yield:

1-(methoxymethoxy)-2-(methylamino)ethane (122225-44-9) + (3R)-3-Benzyloxycarbonyl-3-phenylmethylpropionic acid (116129-80-7) → benzyl (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionate (127944-63-2)

Guidance literature:

With 4-methyl-morpholine; isobutyl chloroformate; Yield given. Multistep reaction; 1.) CH₂Cl₂, -10 deg C, 3 min, 2a.) -10 deg, 15 min, 2b.) RT, 2 h;

DOI:10.1021/jm00169a024

Reference yield: 100.0%

benzyl (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionate (127944-63-2) → (2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionic acid (127944-67-6)

Guidance literature:

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

DOI:10.1021/jm00169a024

upstream raw materials:

1-(methoxymethoxy)-2-(methylamino)ethane

(3R)-3-Benzyloxycarbonyl-3-phenylmethylpropionic acid

2-<<(benzyloxy)carbonyl>methylamino>-1-(methoxymethoxy)ethane

Downstream raw materials:

(2R)-2-benzyl-3-<<<2-(methoxymethoxy)ethyl>methylamino>carbonyl>propionic acid

(R)-2-Benzyl-N¹-[(S)-1-[(1S,2R)-1-cyclohexylmethyl-2-((S)-3-ethyl-2-oxo-oxazolidin-5-yl)-2-hydroxy-ethylcarbamoyl]-2-(3H-imidazol-4-yl)-ethyl]-N⁴-(2-methoxymethoxy-ethyl)-N⁴-methyl-succinamide