2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-{4-[6-(3-fluorooxetan-3-yl)pyridin-3-yl]phenyl}-2-hydroxyethyl]acetamide

Base Information

Chemical Name:2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-{4-[6-(3-fluorooxetan-3-yl)pyridin-3-yl]phenyl}-2-hydroxyethyl]acetamide
CAS No.:1582262-03-0
Molecular Formula:C₁₉H₁₈Cl₂F₂N₂O₃
Molecular Weight:431.266
Hs Code.:

Synonyms:2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-{4-[6-(3-fluorooxetan-3-yl)pyridin-3-yl]phenyl}-2-hydroxyethyl]acetamide

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Chemical Property of 2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-{4-[6-(3-fluorooxetan-3-yl)pyridin-3-yl]phenyl}-2-hydroxyethyl]acetamide

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Technology Process of 2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-{4-[6-(3-fluorooxetan-3-yl)pyridin-3-yl]phenyl}-2-hydroxyethyl]acetamide

There total 4 articles about 2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-{4-[6-(3-fluorooxetan-3-yl)pyridin-3-yl]phenyl}-2-hydroxyethyl]acetamide 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:

: 1582262-98-3
5-{4-[(4S,5R)-3-(dichloroacetyl)-4-(fluoromethyl)-2,2-dimethyl-1,3-oxazolidin-5-yl]phenyl}-2-(3-fluorooxetan-3-yl)pyridine

: 1582262-03-0
2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-{4-[6-(3-fluorooxetan-3-yl)pyridin-3-yl]phenyl}-2-hydroxyethyl]acetamide

Guidance literature:: With water; trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃;

Reference yield:

: 1207758-80-2
3-(5-bromopyridin-2-yl)oxetan-3-ol

: 1582262-03-0
2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-{4-[6-(3-fluorooxetan-3-yl)pyridin-3-yl]phenyl}-2-hydroxyethyl]acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine tris(hydrogen fluoride); ethanaminium,N-(difluoro-λ⁴-sulfanylidene)-N-ethyl-,tetrafluoroborate; triethylamine / dichloromethane / -78 - 0 °C

2.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; sodium carbonate / 1,4-dioxane / 3 h / 80 - 90 °C / Inert atmosphere

2.2: 4 h / 80 - 90 °C / Inert atmosphere

3.1: trifluoroacetic acid; water / dichloromethane / 0 - 20 °C

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; water; potassium acetate; sodium carbonate; triethylamine tris(hydrogen fluoride); triethylamine; ethanaminium,N-(difluoro-λ⁴-sulfanylidene)-N-ethyl-,tetrafluoroborate; trifluoroacetic acid; In 1,4-dioxane; dichloromethane;

Reference yield:

: 624-28-2
2,5-dibromopyridine

: 1582262-03-0
2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-{4-[6-(3-fluorooxetan-3-yl)pyridin-3-yl]phenyl}-2-hydroxyethyl]acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / toluene; hexane / 0.67 h / -78 °C / Inert atmosphere

1.2: 0.5 h / -78 °C

2.1: triethylamine tris(hydrogen fluoride); ethanaminium,N-(difluoro-λ⁴-sulfanylidene)-N-ethyl-,tetrafluoroborate; triethylamine / dichloromethane / -78 - 0 °C

3.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; sodium carbonate / 1,4-dioxane / 3 h / 80 - 90 °C / Inert atmosphere

3.2: 4 h / 80 - 90 °C / Inert atmosphere

4.1: trifluoroacetic acid; water / dichloromethane / 0 - 20 °C

With n-butyllithium; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; water; potassium acetate; sodium carbonate; triethylamine tris(hydrogen fluoride); triethylamine; ethanaminium,N-(difluoro-λ⁴-sulfanylidene)-N-ethyl-,tetrafluoroborate; trifluoroacetic acid; In 1,4-dioxane; hexane; dichloromethane; toluene;