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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402511Generated: October 26, 2026

Diisopropylethylamine → 5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/402511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4,6-Dichloro-5-methylpyrimidineHCID 818860—
Reactant4-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidine hydrochlorideHCID 53400827—
SolventDichloromethaneHCID 6344—
Product5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazoleHCID 8666161143%

Reaction Conditions

Temperature27 °C

Reaction Steps

A solution of 4-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidine hydrochloride (2.0 gm, 0.008369 moles) and diisopropylethylamine (2.78 gm, 0.0215 moles) in dichloromethane (30 ml) was added to an ice-cooled solution of 4,6-dichloro-5-methylpyrimidine (2.1 gm, 0.001295 moles) in dichloromethane (10 ml) and the reaction was stirred at 27° C. for 2 h. The reaction mixture was diluted with dichloromethane and washed with water and brine, dried over sodium sulfate and evaporated under reduced pressure. The crude was purified by flash column chromatography (silica gel, 15% ethyl acetate in hexane) to afford the title compound as a white solid (43% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742117B2
Source datasetuspto-grants-2014_06
ORD IDord-1835680b8e5e4078a7d45ff6eb06ff2d
Source noteuspto-grants-2014_06