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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329402Generated: October 29, 2026

1-(1-Naphthyl)piperazine → HCID 14727008, compound

https://huagongshe.com/reaction/329402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Naphthyl)piperazineHCID 1342—
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 14726987HCID 14726987—
SolventDichloromethaneHCID 6344—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 14727008HCID 14727008—

Reaction Steps

To a 125 ml round-bottomed flask equipped with condenser and N2 inlet were added 2.50 g (7.5 mmol) of 4-(4-(2-chloroethyl)phenyl)-2-methylaminothiazole hydrobromide, 1.59 g (7.5 mmol) of N-(1-naphthyl)piperazine, 1.31 ml (7.5 mmol) of diisopropylethylamine, 1.59 g (15 mmol) of sodium carbonate, 5 mg of sodium iodide, and 50 ml of methylisobutylketone. The reaction was heated at reflux for 4 days, cooled, and the precipitate filtered, and the filtrate evaporated. The residue was taken up in methylene chloride and chromatographed on silica gel using methylene chloride/ethyl acetate as eluent to give an oil. The oil was taken up in methylene chloride, precipitated by addition of methylene chloride saturated with hydrochloride, and the precipitate filtered, washed with ether, and dried to give a white solid, m.p. 272°-273° C., 2.37 g (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04891375
Source datasetuspto-grants-1990_01
ORD IDord-f36e3fc9d03147d98d3252b1eaf16f60
Source noteuspto-grants-1990_01