N-{[6-{4-[3,5-bis(trifluoromethyl)phenyl]-2-oxo-4-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}propanamide

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Chemical Name:N-{[6-{4-[3,5-bis(trifluoromethyl)phenyl]-2-oxo-4-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}propanamide
CAS No.:1365264-92-1
Molecular Formula:C₂₃H₁₇F₁₂N₃O₂
Molecular Weight:595.388
Hs Code.:

Synonyms:N-{[6-{4-[3,5-bis(trifluoromethyl)phenyl]-2-oxo-4-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}propanamide

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Chemical Property of N-{[6-{4-[3,5-bis(trifluoromethyl)phenyl]-2-oxo-4-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}propanamide

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Technology Process of N-{[6-{4-[3,5-bis(trifluoromethyl)phenyl]-2-oxo-4-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}propanamide

There total 6 articles about N-{[6-{4-[3,5-bis(trifluoromethyl)phenyl]-2-oxo-4-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}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:

: 1080630-04-1
N-{[6-{3-[3,5-bis(trifluoromethyl)phenyl]-3-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}propanamide

: 1365264-92-1
N-{[6-{4-[3,5-bis(trifluoromethyl)phenyl]-2-oxo-4-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}propanamide

Guidance literature:: With potassium permanganate; N-benzyl-N,N,N-triethylammonium chloride; In dichloromethane; at 20 ℃; for 75h;

Reference yield:

: 261635-82-9
ethyl 6-chloro-2-(trifluoromethyl)pyridine-3-carboxylate

: 1365264-92-1
N-{[6-{4-[3,5-bis(trifluoromethyl)phenyl]-2-oxo-4-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}propanamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 100 °C

2.1: diisobutylaluminium hydride / dichloromethane; hexane / 0.5 h / -70 °C

2.2: 1 h / 20 °C

3.1: triethylamine; methanesulfonyl chloride / acetonitrile / 1 h / 20 °C / Cooling with ice

3.2: 12 h / 20 °C / Cooling with ice

4.1: triethylamine / dichloromethane / 1 h / 20 °C / Cooling with ice

5.1: N-benzyl-N,N,N-triethylammonium chloride; potassium permanganate / dichloromethane / 75 h / 20 °C

With potassium permanganate; N-benzyl-N,N,N-triethylammonium chloride; diisobutylaluminium hydride; potassium carbonate; methanesulfonyl chloride; triethylamine; In hexane; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1080631-74-8
ethyl 6-{3-[3,5-bis-(trifluoromethyl)phenyl]-3-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)nicotinate

: 1365264-92-1
N-{[6-{4-[3,5-bis(trifluoromethyl)phenyl]-2-oxo-4-(trifluoromethyl)pyrrolidin-1-yl}-2-(trifluoromethyl)pyridin-3-yl]methyl}propanamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: diisobutylaluminium hydride / dichloromethane; hexane / 0.5 h / -70 °C

1.2: 1 h / 20 °C

2.1: triethylamine; methanesulfonyl chloride / acetonitrile / 1 h / 20 °C / Cooling with ice

2.2: 12 h / 20 °C / Cooling with ice

3.1: triethylamine / dichloromethane / 1 h / 20 °C / Cooling with ice

4.1: N-benzyl-N,N,N-triethylammonium chloride; potassium permanganate / dichloromethane / 75 h / 20 °C

With potassium permanganate; N-benzyl-N,N,N-triethylammonium chloride; diisobutylaluminium hydride; methanesulfonyl chloride; triethylamine; In hexane; dichloromethane; acetonitrile;