4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoic acid

Base Information

• Chemical Name: 4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoic acid
• CAS No.: 1573119-81-9
• Molecular Formula: C₂₇H₂₁Cl₃N₂O₅
• Molecular Weight: 559.833
• Mol file: 1573119-81-9.mol

Synonyms:4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoic acid

Chemical Property of 4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoic acid

There total 9 articles about 4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoic acid 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: 84.0%

methyl 4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoate (1374961-91-7) → 4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoic acid (1573119-81-9)

Guidance literature:

With potassium hydroxide; In ethanol; at 20 ℃;

DOI:10.1002/cmdc.201300305

Reference yield:

[3-(2,6-dichlorophenyl)-5-(propan-2-yl)-1,2-oxazol-4-yl]methanol (278597-30-1) → 4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoic acid (1573119-81-9)

Guidance literature:

Multi-step reaction with 4 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

2: potassium hydroxide / ethanol / 20 °C

3: methanesulfonyl chloride / tetrahydrofuran / 0 - 20 °C

4: potassium hydroxide / ethanol / 20 °C

With di-isopropyl azodicarboxylate; methanesulfonyl chloride; triphenylphosphine; potassium hydroxide; In tetrahydrofuran; ethanol;

DOI:10.1002/cmdc.201300305

Reference yield:

2-chloro-4-hydroxybenzonitrile (3336-16-1) → 4-{[2-chloro-4-[[3-(2,6-dichlorophenyl)-5-isopropyl-isoxazol-4-yl]methoxy]benzoyl]amino}benzoic acid (1573119-81-9)

Guidance literature:

Multi-step reaction with 6 steps

1: potassium hydroxide / ethanol / 48 h / Reflux

2: sulfuric acid / 48 h

3: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

4: potassium hydroxide / ethanol / 20 °C

5: methanesulfonyl chloride / tetrahydrofuran / 0 - 20 °C

6: potassium hydroxide / ethanol / 20 °C

With di-isopropyl azodicarboxylate; sulfuric acid; methanesulfonyl chloride; triphenylphosphine; potassium hydroxide; In tetrahydrofuran; ethanol;

DOI:10.1002/cmdc.201300305

upstream raw materials:

[3-(2,6-dichlorophenyl)-5-(propan-2-yl)-1,2-oxazol-4-yl]methanol

2-chloro-4-hydroxybenzonitrile

2-chloro-4-hydroxybenzoic acid

methyl 2-chloro-4-hydroxy-benzoate