(2R,3R)-3-{[2-{[4-(methylsulfonyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-4-yl]oxy}butan-2-ol

Base Information

Chemical Name:(2R,3R)-3-{[2-{[4-(methylsulfonyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-4-yl]oxy}butan-2-ol
CAS No.:1224162-03-1
Molecular Formula:C₁₆H₁₈F₃N₃O₄S
Molecular Weight:405.398
Hs Code.:

Synonyms:(2R,3R)-3-{[2-{[4-(methylsulfonyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-4-yl]oxy}butan-2-ol

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Chemical Property of (2R,3R)-3-{[2-{[4-(methylsulfonyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-4-yl]oxy}butan-2-ol

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Technology Process of (2R,3R)-3-{[2-{[4-(methylsulfonyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-4-yl]oxy}butan-2-ol

There total 3 articles about (2R,3R)-3-{[2-{[4-(methylsulfonyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-4-yl]oxy}butan-2-ol 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: 83.0%

: 1224162-14-4
4-{[(2R,3R)-3-(benzyloxy)butan-2-yl]oxy}-N-[4-(methylsulfonyl)phenyl]-5-(trifluoromethyl)pyrimidin-2-amine

: 1224162-03-1
(2R,3R)-3-{[2-{[4-(methylsulfonyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-4-yl]oxy}butan-2-ol

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In ethanol; at 20 ℃; for 3.25h; under 760.051 Torr;

Reference yield:

: 1223498-47-2
4-{[(1R,2R)-2-(benzyloxy)-1-methylpropyl]oxy}-2-chloro-5-iodopyrimidine

: 1224162-03-1
(2R,3R)-3-{[2-{[4-(methylsulfonyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-4-yl]oxy}butan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1: potassium fluoride; copper(l) iodide / 1-methyl-pyrrolidin-2-one; tetrahydrofuran / 20 - 80 °C

2: acetonitrile / 16 h / 80 °C

3: hydrogen / palladium 10% on activated carbon / ethanol / 3.25 h / 20 °C / 760.05 Torr

With potassium fluoride; copper(l) iodide; hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; ethanol; acetonitrile;

Reference yield:

: 1223498-50-7
4-{[(1R,2R)-2-(benzyloxy)-1-methylpropyl]oxy}-2-chloro-5-(trifluoromethyl)pyrimidine

: 1224162-03-1
(2R,3R)-3-{[2-{[4-(methylsulfonyl)phenyl]amino}-5-(trifluoromethyl)pyrimidin-4-yl]oxy}butan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 16 h / 80 °C

2: hydrogen / palladium 10% on activated carbon / ethanol / 3.25 h / 20 °C / 760.05 Torr

With hydrogen; palladium 10% on activated carbon; In ethanol; acetonitrile;