N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-(cyanomethyl)pyridin-3-yl)propanamide

Base Information

Chemical Name:N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-(cyanomethyl)pyridin-3-yl)propanamide
CAS No.:1419603-08-9
Molecular Formula:C₂₀H₁₅ClF₃N₅O
Molecular Weight:433.82
Hs Code.:

Synonyms:N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-(cyanomethyl)pyridin-3-yl)propanamide

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Chemical Property of N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-(cyanomethyl)pyridin-3-yl)propanamide

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Technology Process of N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-(cyanomethyl)pyridin-3-yl)propanamide

There total 10 articles about N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-(cyanomethyl)pyridin-3-yl)propanamide 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%

: 1254713-79-5
(1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methanamine

: 1419602-73-5
2-(6-cyanopyridin-3-yl)propanoic acid

: 1419603-08-9
N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-(cyanomethyl)pyridin-3-yl)propanamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 23 ℃; Concentration;

Reference yield:

: 14763-20-3
3-chlorophenyl hydrazine

: 1419603-08-9
N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-(cyanomethyl)pyridin-3-yl)propanamide

Guidance literature:: Multi-step reaction with 5 steps

1: ethanol / 3 h / Reflux

2: potassium iodide; isopentyl nitrite / acetonitrile / 20 h / 0 - 1000 °C

3: 1-methyl-pyrrolidin-2-one / 2 h / 200 °C

4: hydrogen; ammonia / methanol / 80 °C / 7500.75 Torr

5: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 23 °C

With ammonia; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; potassium iodide; isopentyl nitrite; In 1-methyl-pyrrolidin-2-one; methanol; ethanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 108-42-9
3-chloro-aniline

: 1419603-08-9
N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-(cyanomethyl)pyridin-3-yl)propanamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogenchloride / water / 0.17 h / -5 - 0 °C

1.2: 5 h / -5 - 0 °C

2.1: ethanol / 5 h / Reflux

3.1: N-chloro-succinimide / N,N-dimethyl-formamide / 3.25 h / 23 °C

4.1: triethylamine / toluene / 20 h / 80 °C

5.1: hydrogen; ammonia / methanol / 80 °C / 7500.75 Torr

6.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / N,N-dimethyl-formamide / 23 °C

With hydrogenchloride; N-chloro-succinimide; ammonia; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In methanol; ethanol; water; N,N-dimethyl-formamide; toluene;