6-oxo-1-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)-1,6-dihydropyrimidin-4-yl trifluoromethanesulfonate

Base Information

Chemical Name:6-oxo-1-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)-1,6-dihydropyrimidin-4-yl trifluoromethanesulfonate
CAS No.:1356353-95-1
Molecular Formula:C₁₆H₁₁F₉N₂O₅S
Molecular Weight:514.325
Hs Code.:

Synonyms:6-oxo-1-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)-1,6-dihydropyrimidin-4-yl trifluoromethanesulfonate

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Chemical Property of 6-oxo-1-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)-1,6-dihydropyrimidin-4-yl trifluoromethanesulfonate

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Technology Process of 6-oxo-1-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)-1,6-dihydropyrimidin-4-yl trifluoromethanesulfonate

There total 5 articles about 6-oxo-1-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)-1,6-dihydropyrimidin-4-yl trifluoromethanesulfonate 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:

: 37595-74-7
N,N-phenylbistrifluoromethane-sulfonimide

: 1356353-94-0
6-hydroxy-3-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)pyrimidin-4(3H)-one

: 1356353-95-1
6-oxo-1-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)-1,6-dihydropyrimidin-4-yl trifluoromethanesulfonate

Guidance literature:: With triethylamine; In tetrahydrofuran; at 0 - 20 ℃;

Reference yield:

: 1356353-93-9
4,4,4-trifluoro-N-[4-(2,2,2-trifluoroethoxy)phenyl]butanimidamide

: 1356353-95-1
6-oxo-1-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)-1,6-dihydropyrimidin-4-yl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methylate / 2-methoxy-ethanol / Reflux

2: triethylamine / tetrahydrofuran / 0 - 20 °C

With sodium methylate; triethylamine; In tetrahydrofuran; 2-methoxy-ethanol;

Reference yield:

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 1356353-95-1
6-oxo-1-[4-(2,2,2-trifluoroethoxy)phenyl]-2-(3,3,3-trifluoropropyl)-1,6-dihydropyrimidin-4-yl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 2 h / 80 °C

2: hydrogen; palladium 10% on activated carbon / water; methanol / 24 h / 20 °C

3: ethanol / 2 h / 20 °C

4: sodium methylate / 2-methoxy-ethanol / Reflux

5: triethylamine / tetrahydrofuran / 0 - 20 °C

With palladium 10% on activated carbon; hydrogen; sodium methylate; potassium carbonate; triethylamine; In tetrahydrofuran; methanol; ethanol; 2-methoxy-ethanol; water; N,N-dimethyl-formamide;