(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)methanol

Base Information

Chemical Name:(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)methanol
CAS No.:1416366-76-1
Molecular Formula:C₂₂H₂₈FN₃O₄S
Molecular Weight:449.546
Hs Code.:

Synonyms:(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)methanol

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Chemical Property of (2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)methanol

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Technology Process of (2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)methanol

There total 12 articles about (2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)methanol 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: 99.0%

: 1416365-05-3
2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidine-5-carbaldehyde

: 1416366-76-1
(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)methanol

Guidance literature:: With sodium tetrahydroborate; In methanol; at 20 ℃; for 0.5h;

Reference yield:

: 1416365-20-2
2-[(3-fluoro-4-{[((1R,2R)-2-{1-[5-(3-furyl)pyrimidin-2-yl]piperidin-4-yl}cyclopropyl)methoxy]methyl}phenyl)sulfonyl]ethanol

: 1416366-76-1
(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)methanol

Guidance literature:: 2-[(3-fluoro-4-{[((1R,2R)-2-{1-[5-(3-furyl)pyrimidin-2-yl]piperidin-4-yl}cyclopropyl)methoxy]methyl}phenyl)sulfonyl]ethanol; With sodium tetrahydroborate; In methanol; at 20 ℃; for 0.166667h; Inert atmosphere;

In methanol;

Reference yield:

: 403802-41-5
tert-butyl 4-(3-hydroxyprop-1-yn-1-yl)piperidine-1-carboxylate

: 1416366-76-1
(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)methanol

Guidance literature:: Multi-step reaction with 8 steps

1.1: hydrogen; quinoline / Lindlar's catalyst / ethyl acetate / 0.67 h / 760.05 Torr

2.1: diethylzinc / dichloromethane; 1,2-dimethoxyethane / 1.58 h / -30 - -20 °C / Inert atmosphere

2.2: 1 h / -15 - 20 °C

3.1: sodium hydride / N,N-dimethyl-formamide / 0.08 h / 0 °C

3.2: 0.5 h / 0 - 20 °C

4.1: n-butyllithium / hexane; diethyl ether / 0.25 h / -78 °C

4.2: 0.5 h / -78 °C

5.1: Oxone / water; methanol / 1 h / 20 °C

6.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 1 h / 20 °C

7.1: caesium carbonate / dimethyl sulfoxide / 20 °C / Inert atmosphere

8.1: sodium tetrahydroborate / methanol / 0.5 h / 20 °C

With quinoline; hydrogenchloride; Oxone; sodium tetrahydroborate; n-butyllithium; hydrogen; diethylzinc; sodium hydride; caesium carbonate; Lindlar's catalyst; In 1,4-dioxane; methanol; 1,2-dimethoxyethane; diethyl ether; hexane; dichloromethane; water; dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide;