3-(4-fluorophenyl)-N-(2-(methylcarbamoyl)phenyl)-4,5-dihydroisoxazole-5-carboxamide

Base Information

• Chemical Name: 3-(4-fluorophenyl)-N-(2-(methylcarbamoyl)phenyl)-4,5-dihydroisoxazole-5-carboxamide
• CAS No.: 1394002-22-2
• Molecular Formula: C₁₈H₁₆FN₃O₃
• Molecular Weight: 341.342
• Mol file: 1394002-22-2.mol

Synonyms:3-(4-fluorophenyl)-N-(2-(methylcarbamoyl)phenyl)-4,5-dihydroisoxazole-5-carboxamide

Chemical Property of 3-(4-fluorophenyl)-N-(2-(methylcarbamoyl)phenyl)-4,5-dihydroisoxazole-5-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-(4-fluorophenyl)-N-(2-(methylcarbamoyl)phenyl)-4,5-dihydroisoxazole-5-carboxamide

There total 3 articles about 3-(4-fluorophenyl)-N-(2-(methylcarbamoyl)phenyl)-4,5-dihydroisoxazole-5-carboxamide 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:

C17H11FN2O3 (1407515-81-4) + methylamine (74-89-5) → 3-(4-fluorophenyl)-N-(2-(methylcarbamoyl)phenyl)-4,5-dihydroisoxazole-5-carboxamide (1394002-22-2)

Guidance literature:

In water; acetonitrile; at 20 ℃;

DOI:10.1016/j.ejmech.2012.06.001

Reference yield:

(E)-4-fluorobenzaldehyde oxime (459-23-4,7304-35-0) → 3-(4-fluorophenyl)-N-(2-(methylcarbamoyl)phenyl)-4,5-dihydroisoxazole-5-carboxamide (1394002-22-2)

Guidance literature:

Multi-step reaction with 3 steps

1: pyridine; N-chloro-succinimide / chloroform / 20 °C / Inert atmosphere; Cooling with ice

2: pyridine; methanesulfonyl chloride / acetonitrile / 20 °C

3: water; acetonitrile / 20 °C

With pyridine; N-chloro-succinimide; methanesulfonyl chloride; In chloroform; water; acetonitrile;

DOI:10.1016/j.ejmech.2012.06.001

Reference yield:

4-fluorobenzaldehyde (459-57-4) → 3-(4-fluorophenyl)-N-(2-(methylcarbamoyl)phenyl)-4,5-dihydroisoxazole-5-carboxamide (1394002-22-2)

Guidance literature:

Multi-step reaction with 4 steps

1: hydroxylamine hydrochloride; sodium acetate / ethanol / 45 - 50 °C

2: pyridine; N-chloro-succinimide / chloroform / 20 °C / Inert atmosphere; Cooling with ice

3: pyridine; methanesulfonyl chloride / acetonitrile / 20 °C

4: water; acetonitrile / 20 °C

With pyridine; N-chloro-succinimide; hydroxylamine hydrochloride; sodium acetate; methanesulfonyl chloride; In ethanol; chloroform; water; acetonitrile;

DOI:10.1016/j.ejmech.2012.06.001

upstream raw materials:

C₁₇H₁₁FN₂O₃

methylamine

(E)-4-fluorobenzaldehyde oxime

4-fluorobenzaldehyde