4-Chloro-2-{2-[3-(thiophen-3-yloxy)-phenyl]-acetylamino}-benzoic acid methyl ester

Base Information

• Chemical Name: 4-Chloro-2-{2-[3-(thiophen-3-yloxy)-phenyl]-acetylamino}-benzoic acid methyl ester
• CAS No.: 1026824-92-9
• Molecular Formula: C₂₀H₁₆ClNO₄S
• Molecular Weight: 401.87
• Mol file: 1026824-92-9.mol

Synonyms:4-Chloro-2-{2-[3-(thiophen-3-yloxy)-phenyl]-acetylamino}-benzoic acid methyl ester

Chemical Property of 4-Chloro-2-{2-[3-(thiophen-3-yloxy)-phenyl]-acetylamino}-benzoic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-Chloro-2-{2-[3-(thiophen-3-yloxy)-phenyl]-acetylamino}-benzoic acid methyl ester

There total 4 articles about 4-Chloro-2-{2-[3-(thiophen-3-yloxy)-phenyl]-acetylamino}-benzoic 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:

3-hydroxy-benzeneacetic acid, methyl ester (42058-59-3) → 4-Chloro-2-{2-[3-(thiophen-3-yloxy)-phenyl]-acetylamino}-benzoic acid methyl ester (1026824-92-9)

Guidance literature:

Multi-step reaction with 4 steps

1: K₂CO₃, CuO / pyridine / 115 °C

2: LiOH, H₂O / methanol / 25 °C

3: (COCl)2 / CH₂Cl₂ / 25 °C

4: 1,2-dichloro-ethane / 80 °C

With lithium hydroxide; oxalyl dichloride; water; potassium carbonate; copper(II) oxide; In pyridine; methanol; dichloromethane; 1,2-dichloro-ethane;

DOI:10.1021/jm00036a002

Reference yield:

[3-(Thiophen-3-yloxy)-phenyl]-acetic acid (155172-85-3) → 4-Chloro-2-{2-[3-(thiophen-3-yloxy)-phenyl]-acetylamino}-benzoic acid methyl ester (1026824-92-9)

Guidance literature:

Multi-step reaction with 2 steps

1: (COCl)2 / CH₂Cl₂ / 25 °C

2: 1,2-dichloro-ethane / 80 °C

With oxalyl dichloride; In dichloromethane; 1,2-dichloro-ethane;

DOI:10.1021/jm00036a002

Reference yield:

[3-(Thiophen-3-yloxy)-phenyl]-acetic acid methyl ester (1026491-17-7) → 4-Chloro-2-{2-[3-(thiophen-3-yloxy)-phenyl]-acetylamino}-benzoic acid methyl ester (1026824-92-9)

Guidance literature:

Multi-step reaction with 3 steps

1: LiOH, H₂O / methanol / 25 °C

2: (COCl)2 / CH₂Cl₂ / 25 °C

3: 1,2-dichloro-ethane / 80 °C

With lithium hydroxide; oxalyl dichloride; water; In methanol; dichloromethane; 1,2-dichloro-ethane;

DOI:10.1021/jm00036a002

upstream raw materials:

2-amino-4-chloro-benzoic acid methyl ester

[3-(Thiophen-3-yloxy)-phenyl]-acetyl chloride

3-hydroxy-benzeneacetic acid, methyl ester

[3-(Thiophen-3-yloxy)-phenyl]-acetic acid