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

Base Information

Chemical Name:4-{[(2R,3R)-3-(benzyloxy)butan-2-yl]oxy}-N-[4-(methylsulfonyl)phenyl]-5-(trifluoromethyl)pyrimidin-2-amine
CAS No.:1224162-14-4
Molecular Formula:C₂₃H₂₄F₃N₃O₄S
Molecular Weight:495.522
Hs Code.:

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

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

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

There total 4 articles about 4-{[(2R,3R)-3-(benzyloxy)butan-2-yl]oxy}-N-[4-(methylsulfonyl)phenyl]-5-(trifluoromethyl)pyrimidin-2-amine 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: 69.0%

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

: 177662-76-9
(4-methylsulfonyl)aniline hydrochloride

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

Guidance literature:: In acetonitrile; at 80 ℃; for 16h;

Reference yield:

: 100-39-0
benzyl bromide

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

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium tert-butylate / tetrahydrofuran / 0.25 h / Reflux

1.2: 20 °C / Reflux

2.1: sodium hydride / diethyl ether; mineral oil / 0.22 h / 0 - 20 °C

2.2: 0 - 40 °C

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

4.1: acetonitrile / 16 h / 80 °C

With potassium fluoride; copper(l) iodide; potassium tert-butylate; sodium hydride; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; diethyl ether; acetonitrile; mineral oil;

Reference yield:

: 124338-52-9
(2R,3R)-3-(phenylmethoxy)-2-butanol

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

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / diethyl ether; mineral oil / 0.22 h / 0 - 20 °C

1.2: 0 - 40 °C

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

3.1: acetonitrile / 16 h / 80 °C

With potassium fluoride; copper(l) iodide; sodium hydride; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; diethyl ether; acetonitrile; mineral oil;