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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600283Generated: October 29, 2026

Piperazine → HCID 45379959, compound

https://huagongshe.com/reaction/600283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTriethylamineHCID 8471—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant3,7-Dichloro-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-oneHCID 45379957—
SolventTetrahydrofuranHCID 8028—
ProductHCID 45379959HCID 4537995972%

Reaction Steps

A solution of 3,7-dichloro-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-one (193 mg, 0.64 mmol), piperazine (118 mg, 0.91 mmol, Aldrich) and triethylamine (0.15 mL, 1.07 mmol) in THF (3 mL) was stirred at room temperature for one hour. The reaction was partitioned between ethyl acetate and water. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, and solvent was removed at reduced pressure to give a brown oil. This was passed through a column of silica gel with 80-100% ethyl acetate/hexane to give 7-chloro-3-(piperazin-1-yl)-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-one. (183 mg, 72% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902195B2
Source datasetuspto-grants-2011_03
ORD IDord-07b5e88de17046c1b90006367b2852db
Source noteuspto-grants-2011_03