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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749106Generated: October 31, 2026

Piperazine → HCID 66965559, compound

https://huagongshe.com/reaction/749106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 23032566HCID 23032566—
SolventEthylene GlycolHCID 174—
ProductHCID 66965559HCID 66965559—

Reaction Conditions

Temperature200 °C

Reaction Steps

To a suspension of 4-chloro-5,6,7,8-tetrahydrophthalazin-1(2H)-one (150 mg; CAS Registry No. 89981-21-5; the compound described in Yakugaku Zassi., 82, 302-303 (1962)) in ethylene glycol (1.6 mL) was added piperazine (420 mg) and the mixture was stirred at 200° C. for 7 hours. After cooling to room temperature, the reaction mixture was poured in a cold saturated aqueous sodium hydrogen carbonate solution and extracted with chloroform. The extract was washed brine, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by column chromatography on silica gel (methylene chloride:methanol=20:1→10:1) to give free form of the title compound (64 mg). To a solution of the obtained free form in methanol (2.0 mL) was added 4N hydrogen chloride-ethyl acetate solution (1 mL). The mixture was stirred at room temperature and concentrated. The residue was recrystallized from a mixed solution of methanol and ethyl acetate to give the compound of the present invention (21 mg) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402580B2
Source datasetuspto-grants-2008_07
ORD IDord-48166eec7755427aac21ac353a4b51e2
Source noteuspto-grants-2008_07