N-(2-oxoindolin-6-ylcarbamoyl)-4-(trifluoromethyl)benzamide

Base Information

• Chemical Name: N-(2-oxoindolin-6-ylcarbamoyl)-4-(trifluoromethyl)benzamide
• CAS No.: 1621584-39-1
• Molecular Formula: C₁₇H₁₂F₃N₃O₃
• Molecular Weight: 363.296
• Mol file: 1621584-39-1.mol

Synonyms:N-(2-oxoindolin-6-ylcarbamoyl)-4-(trifluoromethyl)benzamide

Chemical Property of N-(2-oxoindolin-6-ylcarbamoyl)-4-(trifluoromethyl)benzamide

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:

Useful:

Technology Process of N-(2-oxoindolin-6-ylcarbamoyl)-4-(trifluoromethyl)benzamide

There total 4 articles about N-(2-oxoindolin-6-ylcarbamoyl)-4-(trifluoromethyl)benzamide 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: 89.0%

6-amino-1,3-dihydro-indol-2-one (150544-04-0) + 4-(trifluoromethyl)benzoyl isocyanate (125931-36-4) → N-(2-oxoindolin-6-ylcarbamoyl)-4-(trifluoromethyl)benzamide (1621584-39-1)

Guidance literature:

In acetonitrile; at 70 - 80 ℃;

DOI:10.1016/j.ejmech.2014.07.108

Reference yield:

(2,4-dinitro-phenyl)-acetic acid (643-43-6) → N-(2-oxoindolin-6-ylcarbamoyl)-4-(trifluoromethyl)benzamide (1621584-39-1)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrogen; palladium on activated charcoal / methanol

2: hydrogenchloride / water / 6 h / Reflux

3: acetonitrile / 70 - 80 °C

With hydrogenchloride; palladium on activated charcoal; hydrogen; In methanol; water; acetonitrile;

DOI:10.1016/j.ejmech.2014.07.108

Reference yield:

2,4-diaminophenylacetic acid (79637-84-6) → N-(2-oxoindolin-6-ylcarbamoyl)-4-(trifluoromethyl)benzamide (1621584-39-1)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride / water / 6 h / Reflux

2: acetonitrile / 70 - 80 °C

With hydrogenchloride; In water; acetonitrile;

DOI:10.1016/j.ejmech.2014.07.108

upstream raw materials:

p-trifluoromethylbenzamide

(2,4-dinitro-phenyl)-acetic acid

2,4-diaminophenylacetic acid

6-amino-1,3-dihydro-indol-2-one