(4'-methoxy-biphenyl-4-sulfonylamino)-[1-(2-methoxy-ethoxycarbonyl)-piperidin-4-yl]-acetic acid methyl ester

Base Information

• Chemical Name: (4'-methoxy-biphenyl-4-sulfonylamino)-[1-(2-methoxy-ethoxycarbonyl)-piperidin-4-yl]-acetic acid methyl ester
• CAS No.: 357413-57-1
• Molecular Formula: C₂₅H₃₂N₂O₈S
• Molecular Weight: 520.604
• Mol file: 357413-57-1.mol

Synonyms:(4'-methoxy-biphenyl-4-sulfonylamino)-[1-(2-methoxy-ethoxycarbonyl)-piperidin-4-yl]-acetic acid methyl ester

Chemical Property of (4'-methoxy-biphenyl-4-sulfonylamino)-[1-(2-methoxy-ethoxycarbonyl)-piperidin-4-yl]-acetic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (4'-methoxy-biphenyl-4-sulfonylamino)-[1-(2-methoxy-ethoxycarbonyl)-piperidin-4-yl]-acetic acid methyl ester

There total 5 articles about (4'-methoxy-biphenyl-4-sulfonylamino)-[1-(2-methoxy-ethoxycarbonyl)-piperidin-4-yl]-acetic acid methyl 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-tert-butyloxycarbonylpiperidin-4-one (79099-07-3) → (4'-methoxy-biphenyl-4-sulfonylamino)-[1-(2-methoxy-ethoxycarbonyl)-piperidin-4-yl]-acetic acid methyl ester (357413-57-1)

Guidance literature:

Multi-step reaction with 5 steps

1: 93.2 percent / diazabicycloundecane / CH₂Cl₂ / 2 h / 20 °C

2: H₂ / Pd/C / methanol / 12 h / 20 °C / 2327.23 Torr

3: 8.22 g / triethylamine / CH₂Cl₂ / 20 °C

4: trifluoroacetic acid / CH₂Cl₂ / 20 °C

5: 5.24 g / triethylamine / CH₂Cl₂ / 4 h / 20 °C

With diazabicycloundecane; hydrogen; triethylamine; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane;

DOI:10.1021/jm015531s

Reference yield:

4-(benzyloxycarbonylamino-methoxycarbonyl-methylene)-piperidine-1-carboxylic acid tert-butyl ester (313491-20-2) → (4'-methoxy-biphenyl-4-sulfonylamino)-[1-(2-methoxy-ethoxycarbonyl)-piperidin-4-yl]-acetic acid methyl ester (357413-57-1)

Guidance literature:

Multi-step reaction with 4 steps

1: H₂ / Pd/C / methanol / 12 h / 20 °C / 2327.23 Torr

2: 8.22 g / triethylamine / CH₂Cl₂ / 20 °C

3: trifluoroacetic acid / CH₂Cl₂ / 20 °C

4: 5.24 g / triethylamine / CH₂Cl₂ / 4 h / 20 °C

With hydrogen; triethylamine; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane;

DOI:10.1021/jm015531s

Reference yield:

2-Methoxyethyl chloroformate (628-12-6) + (4'-methoxy-biphenyl-4-sulfonylamino)-piperidin-4-yl-acetic acid methyl ester → (4'-methoxy-biphenyl-4-sulfonylamino)-[1-(2-methoxy-ethoxycarbonyl)-piperidin-4-yl]-acetic acid methyl ester (357413-57-1)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; for 4h;

DOI:10.1021/jm015531s

upstream raw materials:

2-Methoxyethyl chloroformate

N-tert-butyloxycarbonylpiperidin-4-one

tert-butyl 4-(1-amino-2-methoxy-2-oxoethyl)piperidine-1-carboxylate

4-(benzyloxycarbonylamino-methoxycarbonyl-methylene)-piperidine-1-carboxylic acid tert-butyl ester