2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (3-ethyl-5-trifluoromethyl-indol-1-yl)-amide

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Chemical Name:2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (3-ethyl-5-trifluoromethyl-indol-1-yl)-amide
CAS No.:1068971-10-7
Molecular Formula:C₂₃H₁₈F₄N₄O
Molecular Weight:442.416
Hs Code.:

Synonyms:2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (3-ethyl-5-trifluoromethyl-indol-1-yl)-amide

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Chemical Property of 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (3-ethyl-5-trifluoromethyl-indol-1-yl)-amide

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Technology Process of 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (3-ethyl-5-trifluoromethyl-indol-1-yl)-amide

There total 8 articles about 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (3-ethyl-5-trifluoromethyl-indol-1-yl)-amide 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: 54.0%

: 933989-07-2
2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid

: 1068975-76-7
3-ethyl-5-trifluoromethyl-1H-indol-1-ylamine

: 1068971-10-7
2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (3-ethyl-5-trifluoromethyl-indol-1-yl)-amide

Guidance literature:: 2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid; 3-ethyl-5-trifluoromethyl-1H-indol-1-ylamine; In N,N-dimethyl-formamide; at 50 ℃; for 1h;

With 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In N,N-dimethyl-formamide; at 50 ℃; for 2h;

Reference yield:

: 878133-04-1
2,2,2-trifluoro-N-(2-iodo-4-(trifluoromethyl)phenyl)acetamide

: 1068971-10-7
2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (3-ethyl-5-trifluoromethyl-indol-1-yl)-amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetonitrile / 2 h / Heating / reflux

2.1: tetrabutyl-ammonium chloride / palladium diacetate / N,N-dimethyl-formamide / 2 h / 100 °C

3.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 °C

3.2: 2 h / 0 - 20 °C

3.3: 0 °C

4.1: N,N-dimethyl-formamide / 1 h / 50 °C

4.2: 2 h / 50 °C

With tetrabutyl-ammonium chloride; sodium hydride; potassium carbonate; palladium diacetate; In N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1068975-72-3
N-but-2-enyl-2,2,2-trifluoro-N-(2-iodo-4-trifluoromethyl-phenyl)-acetamide

: 1068971-10-7
2-(3-fluoro-phenyl)-4-methyl-pyrimidine-5-carboxylic acid (3-ethyl-5-trifluoromethyl-indol-1-yl)-amide

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrabutyl-ammonium chloride / palladium diacetate / N,N-dimethyl-formamide / 2 h / 100 °C

2.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 °C

2.2: 2 h / 0 - 20 °C

2.3: 0 °C

3.1: N,N-dimethyl-formamide / 1 h / 50 °C

3.2: 2 h / 50 °C

With tetrabutyl-ammonium chloride; sodium hydride; palladium diacetate; In N,N-dimethyl-formamide;