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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515245Generated: October 29, 2026

Dichloromethane → 2-(4-(6-Chloro-2-methylpyrimidin-4-yl)piperazin-1-yl)ethanol

https://huagongshe.com/reaction/515245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
Reactant4,6-Dichloro-2-methylpyrimidineHCID 234997—
SolventTriethylamineHCID 8471—
Product2-(4-(6-Chloro-2-methylpyrimidin-4-yl)piperazin-1-yl)ethanolHCID 1447955889.8%

Reaction Conditions

Temperature30 °C

Reaction Steps

1-(2-hydroxyethyl)piperazine (Compound 3) (16.6 g, 127.6 mmol)) and 2-methyl-4,6-dichloropyrimidine (Compound 2) (10.4 g, 63.8 mmol) were mixed with methylene dichloride (80 mL) in reaction flask to be stirred for 2.5 h at 30° C., and then triethylamine (1.8 mL) was added with the reaction overnight in thermal insulation. After vacuum filtration, the cake was rinsed by methylene dichloride. The filtrate was vacuum condensed to dry, and then n-hexane (40 mL) was added to grow the grains for 1 h by stirring. After vacuum filtration, the cake was rinsed by n-hexane (20 mL) and dried at 40° C. to constant weight to give white solid target Compound 4 (14.7 g, yield: 89.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108954B2
Source datasetuspto-grants-2015_08
ORD IDord-9c2895924dc74897ab2ed8b4c70ac49f
Source noteuspto-grants-2015_08