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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358607Generated: October 28, 2026

Water → HCID 18185391, compound

https://huagongshe.com/reaction/1358607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 18185381HCID 18185381—
SolventSodium BicarbonateHCID 516892—
ProductHCID 18185391HCID 1818539167%

Reaction Steps

2-Chloro-5-(4,4-dimethyl-4,5-dihydro-oxazol-2-yl)-pyridine hydrochloride was transformed into its free base by dissolving 8.0 g (32 mmol) in saturated sodium bicarbonate solution and extracting the base into dichloromethane. The solvent was evaporated and the residue was dissolved in toluene. After addition of 11.35 g (113 mmol) N-methylpiperazine, the mixture was refluxed for 36 h. After cooling to room temperature water (50 ml) and ethyl acetate (150 ml) were added and the aqueous layer was extracted with ethyl acetate (150 ml). The combined organic layers were extracted two times with 1 N hydrochloric acid, the acidic aqueous layer was made alkaline with 28% sodium hydroxide solution and extracted two times with dichloromethane. The organic layer was dried (magnesium sulfate) and evaporated. The residue was crystallized from ethyl acetate/hexane to yield 6.0 g (67%) of a white crystalline compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596773B2
Source datasetuspto-grants-2003_07
ORD IDord-bba90c51959c4156bf741744ad52b580
Source noteuspto-grants-2003_07