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

Base Information

Chemical Name:N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-((2-hydroxyethyl)(methyl)amino)pyridin-3-yl)propanamide
CAS No.:1419601-41-4
Molecular Formula:C₂₂H₂₃ClF₃N₅O₂
Molecular Weight:481.905
Hs Code.:

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

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

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

There total 11 articles about N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-((2-hydroxyethyl)(methyl)amino)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: 68.0%

: 1419599-61-3
N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-((2-methoxyethyl)(methyl)amino)pyridin-3-yl)propanamide

: 1419601-41-4
N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-((2-hydroxyethyl)(methyl)amino)pyridin-3-yl)propanamide

Guidance literature:: With boron tribromide; In dichloromethane; at -78 - 23 ℃; for 3h;

Reference yield:

: 14763-20-3
3-chlorophenyl hydrazine

: 1419601-41-4
N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-((2-hydroxyethyl)(methyl)amino)pyridin-3-yl)propanamide

Guidance literature:: Multi-step reaction with 6 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; N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 3 h / 23 °C

6: boron tribromide / dichloromethane / 3 h / -78 - 23 °C

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

Reference yield:

: 39891-09-3
(6-chloro-pyridin-3-yl)-acetonitrile

: 1419601-41-4
N-((1-(3-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl)methyl)-2-(6-((2-hydroxyethyl)(methyl)amino)pyridin-3-yl)propanamide

Guidance literature:: Multi-step reaction with 6 steps

1: sodium hydride / tetrahydrofuran / 0.17 h / 0 °C

2: triethylamine / dimethyl sulfoxide / 16 h / 100 °C

3: chloro-trimethyl-silane / 5 h / 60 °C

4: lithium hydroxide monohydrate; water / tetrahydrofuran / 2 h / 60 °C

5: benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 3 h / 23 °C

6: boron tribromide / dichloromethane / 3 h / -78 - 23 °C

With chloro-trimethyl-silane; lithium hydroxide monohydrate; water; boron tribromide; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;