N-[2-amino-4-benzyloxy-5-methoxybenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine

Base Information

• Chemical Name: N-[2-amino-4-benzyloxy-5-methoxybenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine
• CAS No.: 864665-79-2
• Molecular Formula: C₂₀H₂₄N₂O₅
• Molecular Weight: 372.421
• Mol file: 864665-79-2.mol

Synonyms:N-[2-amino-4-benzyloxy-5-methoxybenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine

Chemical Property of N-[2-amino-4-benzyloxy-5-methoxybenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-[2-amino-4-benzyloxy-5-methoxybenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine

There total 3 articles about N-[2-amino-4-benzyloxy-5-methoxybenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine 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-[4-benzyloxy-5-methoxy-2-nitrobenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine (864665-78-1) → N-[2-amino-4-benzyloxy-5-methoxybenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine (864665-79-2)

Guidance literature:

With methanol; tin(ll) chloride; for 3h; Heating / reflux;

Reference yield:

4-(benzyloxy)-5-methoxy-2-nitrobenzoic acid (60547-92-4) → N-[2-amino-4-benzyloxy-5-methoxybenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine (864665-79-2)

Guidance literature:

Multi-step reaction with 4 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 16 h / 20 °C / Inert atmosphere

2: triethylamine / dichloromethane / 16 h / -20 - 20 °C / Inert atmosphere

3: lithium borohydride / tetrahydrofuran / 4.5 h / 0 - 20 °C / Inert atmosphere

4: tin(II) chloride dihdyrate; methanol / 3 h / Reflux

With methanol; lithium borohydride; oxalyl dichloride; tin(II) chloride dihdyrate; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane;

DOI:10.1021/acs.jmedchem.7b00736

Reference yield:

4-benzyloxy-5-methoxy-2-nitrobenzoyl chloride (64154-78-5) → N-[2-amino-4-benzyloxy-5-methoxybenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine (864665-79-2)

Guidance literature:

Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 16 h / -20 - 20 °C / Inert atmosphere

2: lithium borohydride / tetrahydrofuran / 4.5 h / 0 - 20 °C / Inert atmosphere

3: tin(II) chloride dihdyrate; methanol / 3 h / Reflux

With methanol; lithium borohydride; tin(II) chloride dihdyrate; triethylamine; In tetrahydrofuran; dichloromethane;

DOI:10.1021/acs.jmedchem.7b00736

upstream raw materials:

N-[4-benzyloxy-5-methoxy-2-nitrobenzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine

4-(benzyloxy)-5-methoxy-2-nitrobenzoic acid

4-benzyloxy-5-methoxy-2-nitrobenzoyl chloride

Downstream raw materials:

N-[4-benzyloxy-5-methoxy-2-(tert-butyloxycarbonylamino)benzoyl]-(2S,4R)-4-hydroxy-2-(hydroxymethyl)pyrrolidine