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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161664Generated: October 27, 2026

Water → 1-(2-Chloro-6-phenyl-pyrimidin-4-yl)-piperidin-4-ol

https://huagongshe.com/reaction/1161664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantPiperidin-4-olHCID 79341—
Reactant2,4-Dichloro-6-phenylpyrimidineHCID 241554—
Solvent1-ButanolHCID 263—
Product1-(2-Chloro-6-phenyl-pyrimidin-4-yl)-piperidin-4-olHCID 58626078—
Product1-(4-Chloro-6-phenyl-pyrimidin-2-yl)-piperidin-4-olHCID 58626127—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of compound, 2,4-dichloro-6-phenyl-pyrimidine (13 g, 57.77 mmol), piperidin-4-ol (2.9 g, 28.88 mmol) and triethylamine (32.14 mL, 231.11 mmol) in butanol (110 mL) was stirred at 120° C. for 12 hours under nitrogen atmosphere. The reaction mixture was then poured into water (250 mL) and extracted with ethyl acetate (3×50 mL). The organic layers were collected, combined, washed with water (50 mL), dried over anhydrous sodium sulphate, and concentrated under vacuum. The residue thus obtained was purified by column chromatography using ethyl acetate-petroleum ether to give the two compounds, 1-(4-chloro-6-phenyl-pyrimidin-2-yl)-piperidin-4-ol and 1-(2-chloro-6-phenyl-pyrimidin-4-yl)-piperidin-4-ol in ratio 1:4 (overall yield: 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820654B2
Source datasetuspto-grants-2010_10
ORD IDord-58b9974ee23e462f936c2eca623109c8
Source noteuspto-grants-2010_10