6-(1-(2,6-difluorophenyl)propyl)-5-methyl-2-(methylthio)pyrimidin-4(3H)-one

Base Information

Chemical Name:6-(1-(2,6-difluorophenyl)propyl)-5-methyl-2-(methylthio)pyrimidin-4(3H)-one
CAS No.:1320339-96-5
Molecular Formula:C₁₅H₁₆F₂N₂OS
Molecular Weight:310.368
Hs Code.:

Synonyms:6-(1-(2,6-difluorophenyl)propyl)-5-methyl-2-(methylthio)pyrimidin-4(3H)-one

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Chemical Property of 6-(1-(2,6-difluorophenyl)propyl)-5-methyl-2-(methylthio)pyrimidin-4(3H)-one

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Technology Process of 6-(1-(2,6-difluorophenyl)propyl)-5-methyl-2-(methylthio)pyrimidin-4(3H)-one

There total 5 articles about 6-(1-(2,6-difluorophenyl)propyl)-5-methyl-2-(methylthio)pyrimidin-4(3H)-one 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: 60.0%

: 6-(1-(2,6-difluoro-phenyl)-propyl)-5-methyl-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one

: 74-88-4
methyl iodide

: 1320339-96-5
6-(1-(2,6-difluorophenyl)propyl)-5-methyl-2-(methylthio)pyrimidin-4(3H)-one

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/jm200734j

Reference yield:

: 958237-61-1
4-(2,6-dichlorophenyl)-2-methyl-3-oxo-hexanoic acid ethyl ester

: 1320339-96-5
6-(1-(2,6-difluorophenyl)propyl)-5-methyl-2-(methylthio)pyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: sodium / ethanol / Reflux

2: potassium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C / Inert atmosphere

With sodium; potassium carbonate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm200734j

Reference yield:

: 359828-70-9
2-(2,6-difluorophenyl)butanoic acid

: 1320339-96-5
6-(1-(2,6-difluorophenyl)propyl)-5-methyl-2-(methylthio)pyrimidin-4(3H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: acetonitrile

2: triethylamine; magnesium chloride / acetonitrile

3: sodium / ethanol / Reflux

4: potassium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C / Inert atmosphere

With sodium; potassium carbonate; triethylamine; magnesium chloride; In ethanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm200734j