N-(1-(4-fluorophenyl)piperidin-4-yl)-3-hydroxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide

Base Information

Chemical Name:N-(1-(4-fluorophenyl)piperidin-4-yl)-3-hydroxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide
CAS No.:1429216-25-0
Molecular Formula:C₁₉H₁₉F₄N₃O₃
Molecular Weight:413.372
Hs Code.:

Synonyms:N-(1-(4-fluorophenyl)piperidin-4-yl)-3-hydroxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide

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Chemical Property of N-(1-(4-fluorophenyl)piperidin-4-yl)-3-hydroxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide

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Technology Process of N-(1-(4-fluorophenyl)piperidin-4-yl)-3-hydroxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide

There total 7 articles about N-(1-(4-fluorophenyl)piperidin-4-yl)-3-hydroxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide 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: 72.0%

: 1429217-44-6
N-(1-(4-fluorophenyl)piperidin-4-yl)-3-methoxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide

: 1429216-25-0
N-(1-(4-fluorophenyl)piperidin-4-yl)-3-hydroxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide

Guidance literature:: With boron trichloride - methyl sulfide complex; In dichloromethane; 1,2-dichloro-ethane; at 70 ℃; for 3h;

Reference yield:

: 1429217-39-9
ethyl 3-methoxy-2-oxo-1,2-dihydropyridine-4-carboxylate

: 1429216-25-0
N-(1-(4-fluorophenyl)piperidin-4-yl)-3-hydroxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: caesium carbonate / dichloromethane / 0.17 h / 60 °C

1.2: 16 h / 20 °C

2.1: sodium hydroxide; lithium hydroxide / 16 h / 50 °C

3.1: thionyl chloride / 2 h / 70 °C

4.1: triethylamine / dichloromethane / 3 h / 20 °C

5.1: boron trichloride - methyl sulfide complex / dichloromethane; 1,2-dichloro-ethane / 3 h / 70 °C

With thionyl chloride; boron trichloride - methyl sulfide complex; caesium carbonate; triethylamine; sodium hydroxide; lithium hydroxide; In dichloromethane; 1,2-dichloro-ethane;

Reference yield:

: 1429217-41-3
ethyl 3-methoxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxylate

: 1429216-25-0
N-(1-(4-fluorophenyl)piperidin-4-yl)-3-hydroxy-2-oxo-1-(2,2,2-trifluoroethyl)-1,2-dihydropyridine-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydroxide; lithium hydroxide / 16 h / 50 °C

2: thionyl chloride / 2 h / 70 °C

3: triethylamine / dichloromethane / 3 h / 20 °C

4: boron trichloride - methyl sulfide complex / dichloromethane; 1,2-dichloro-ethane / 3 h / 70 °C

With thionyl chloride; boron trichloride - methyl sulfide complex; triethylamine; sodium hydroxide; lithium hydroxide; In dichloromethane; 1,2-dichloro-ethane;