(2R,3R)-3-[2-(4-Cyclopropanesulphonylphenylamino)-5-trifluoromethylpyrimidin-4-yloxy]butan-2-ol

Base Information

• Chemical Name: (2R,3R)-3-[2-(4-Cyclopropanesulphonylphenylamino)-5-trifluoromethylpyrimidin-4-yloxy]butan-2-ol
• CAS No.: 1224162-02-0
• Molecular Formula: C₁₈H₂₀F₃N₃O₄S
• Molecular Weight: 431.436
• Mol file: 1224162-02-0.mol

Synonyms:(2R,3R)-3-[2-(4-Cyclopropanesulphonylphenylamino)-5-trifluoromethylpyrimidin-4-yloxy]butan-2-ol

Chemical Property of (2R,3R)-3-[2-(4-Cyclopropanesulphonylphenylamino)-5-trifluoromethylpyrimidin-4-yloxy]butan-2-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R,3R)-3-[2-(4-Cyclopropanesulphonylphenylamino)-5-trifluoromethylpyrimidin-4-yloxy]butan-2-ol

There total 6 articles about (2R,3R)-3-[2-(4-Cyclopropanesulphonylphenylamino)-5-trifluoromethylpyrimidin-4-yloxy]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: 39.0%

[4-((1R,2R)-2-Benzyloxy-1-methylpropoxy)-5-trifluoromethylpyrimidin-2-yl](4-cyclopropane-sulphonylphenyl)amine (1224162-13-3) → (2R,3R)-3-[2-(4-Cyclopropanesulphonylphenylamino)-5-trifluoromethylpyrimidin-4-yloxy]butan-2-ol (1224162-02-0)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In ethanol; at 20 ℃; for 1h; under 760.051 Torr;

Reference yield:

1-(cyclopropylsulphanyl)-4-nitrobenzene (851008-48-5) → (2R,3R)-3-[2-(4-Cyclopropanesulphonylphenylamino)-5-trifluoromethylpyrimidin-4-yloxy]butan-2-ol (1224162-02-0)

Guidance literature:

Multi-step reaction with 4 steps

1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C

2: hydrogen / Raney nickel / ethanol; tetrahydrofuran / 1.5 h / 0 °C / 760.05 Torr

3: hydrogenchloride / 1,4-dioxane; acetonitrile / 5.5 h / 80 °C

4: hydrogen / palladium 10% on activated carbon / ethanol / 1 h / 20 °C / 760.05 Torr

With hydrogenchloride; hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; acetonitrile;

Reference yield:

1-(cyclopropylsulfonyl)-4-nitrobenzene (19433-07-9) → (2R,3R)-3-[2-(4-Cyclopropanesulphonylphenylamino)-5-trifluoromethylpyrimidin-4-yloxy]butan-2-ol (1224162-02-0)

Guidance literature:

Multi-step reaction with 3 steps

1: hydrogen / Raney nickel / ethanol; tetrahydrofuran / 1.5 h / 0 °C / 760.05 Torr

2: hydrogenchloride / 1,4-dioxane; acetonitrile / 5.5 h / 80 °C

3: hydrogen / palladium 10% on activated carbon / ethanol / 1 h / 20 °C / 760.05 Torr

With hydrogenchloride; hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; ethanol; acetonitrile;

upstream raw materials:

4-Fluoronitrobenzene

1-(cyclopropylsulphanyl)-4-nitrobenzene

4-(cyclopropylsulfonyl)aniline

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