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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635210Generated: October 30, 2026

2,4-Dichloro-6-methylpyrimidine → HCID 15512220, compound

https://huagongshe.com/reaction/635210

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6-methylpyrimidineHCID 79471—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Phenyl-1,2,3,6-tetrahydropyridine hydrochlorideHCID 2723860—
SolventEthanolHCID 702—
ProductHCID 15512220HCID 1551222067.5%

Reaction Steps

In 4 ml of ethanol was dissolved 415 mg of 2,4-dichloro-6-methylpyrimidine, and the solution was cooled with ice-water. To the solution were added 503 mg of 4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride and 664 mg of diisopropylethylamine, followed by stirring overnight under cooling with ice. The reaction solution was poured into a saturated aqueous solution of sodium hydrogencarbonate and extracted with ethyl acetate. The extract was washed with a saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The desiccant was removed by filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=10/1 to 3/1) to give 491 mg of 4-(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)-2-chloro-6-methylpyrimidine as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187781B1
Source datasetuspto-grants-2001_02
ORD IDord-b7143ff13d6141cfb09569a48565fd3a
Source noteuspto-grants-2001_02