5-bromo-2-(4-cyanobenzoyl)-3-(5-methylisoxazol-4-carbonyl)-aminobenzo[b]furan

Base Information

• Chemical Name: 5-bromo-2-(4-cyanobenzoyl)-3-(5-methylisoxazol-4-carbonyl)-aminobenzo[b]furan
• CAS No.: 636992-63-7
• Molecular Formula: C₂₁H₁₂BrN₃O₄
• Molecular Weight: 450.248
• Mol file: 636992-63-7.mol

Synonyms:5-bromo-2-(4-cyanobenzoyl)-3-(5-methylisoxazol-4-carbonyl)-aminobenzo[b]furan

Chemical Property of 5-bromo-2-(4-cyanobenzoyl)-3-(5-methylisoxazol-4-carbonyl)-aminobenzo[b]furan

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-bromo-2-(4-cyanobenzoyl)-3-(5-methylisoxazol-4-carbonyl)-aminobenzo[b]furan

There total 3 articles about 5-bromo-2-(4-cyanobenzoyl)-3-(5-methylisoxazol-4-carbonyl)-aminobenzo[b]furan 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: 34.0%

5-methyl-3-isoxazolyl chloride (39499-34-8) + 4-(3-amino-5-bromo-benzofuran-2-carbonyl)-benzonitrile (636992-59-1) → 5-bromo-2-(4-cyanobenzoyl)-3-(5-methylisoxazol-4-carbonyl)-aminobenzo[b]furan (636992-63-7)

Guidance literature:

In tetrahydrofuran; at 65 ℃; for 7h;

DOI:10.1039/b307468d

Reference yield:

4-(2-chloroacetyl)benzenecarbonitrile (40805-50-3) → 5-bromo-2-(4-cyanobenzoyl)-3-(5-methylisoxazol-4-carbonyl)-aminobenzo[b]furan (636992-63-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 76 percent / K₂CO₃

2: 34 percent / tetrahydrofuran / 7 h / 65 °C

With potassium carbonate; In tetrahydrofuran;

DOI:10.1039/b307468d

Reference yield:

5-bromo-2-hydroxybenzonitrile (40530-18-5) → 5-bromo-2-(4-cyanobenzoyl)-3-(5-methylisoxazol-4-carbonyl)-aminobenzo[b]furan (636992-63-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 76 percent / K₂CO₃

2: 34 percent / tetrahydrofuran / 7 h / 65 °C

With potassium carbonate; In tetrahydrofuran;

DOI:10.1039/b307468d

upstream raw materials:

5-methyl-3-isoxazolyl chloride

4-(3-amino-5-bromo-benzofuran-2-carbonyl)-benzonitrile

5-bromo-2-hydroxybenzonitrile

4-(2-chloroacetyl)benzenecarbonitrile