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

Base Information

Chemical Name:1-(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)ethanol
CAS No.:1416366-77-2
Molecular Formula:C₂₃H₃₀FN₃O₄S
Molecular Weight:463.573
Hs Code.:

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

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

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

There total 10 articles about 1-(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)ethanol 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: 100.0%

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

: 676-58-4
methylmagnesium chloride

: 1416366-77-2
1-(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)ethanol

Guidance literature:: In tetrahydrofuran; at 0 - 20 ℃; for 0.5h; Inert atmosphere;

Reference yield:

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

: 1416366-77-2
1-(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)ethanol

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: tetrahydrofuran / 0.5 h / 0 - 20 °C / Inert atmosphere

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

Reference yield:

: tert-butyl 4-[(1Z)-3-hydroxyprop-1-en-1-yl]piperidine-1-carboxylate

: 1416366-77-2
1-(2-(4-((1R,2R)-2-(((2-fluoro-4-(methylsulfonyl)benzyl)oxy)methyl)cyclopropyl)piperidin-1-yl)pyrimidin-5-yl)ethanol

Guidance literature:: Multi-step reaction with 7 steps

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

1.2: 1 h / -15 - 20 °C

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

2.2: 0.5 h / 0 - 20 °C

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

3.2: 0.5 h / -78 °C

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

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

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

7.1: tetrahydrofuran / 0.5 h / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; Oxone; n-butyllithium; diethylzinc; sodium hydride; caesium carbonate; In tetrahydrofuran; 1,4-dioxane; methanol; 1,2-dimethoxyethane; diethyl ether; hexane; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;