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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207820Generated: November 2, 2026

Acetyl chloride → 1-(4-(3-((1-(Quinolin-2-yl)piperidin-4-yl)oxy)pyrazin-2-yl)piperazin-1-yl)ethanone

https://huagongshe.com/reaction/2207820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant2-(4-((3-(Piperazin-1-YL)pyrazin-2-YL)oxy)piperidin-1-YL)quinolineHCID 67477433—
SolventDichloromethaneHCID 6344—
Product1-(4-(3-((1-(Quinolin-2-yl)piperidin-4-yl)oxy)pyrazin-2-yl)piperazin-1-yl)ethanoneHCID 5467067278%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(4-((3-(piperazin-1-yl)pyrazin-2-yl)oxy)piperidin-1-yl)quinoline (130 mg, 0.33 mmol) in dry DCM (10 mL) was added Et3N (1 mL). The reaction mixture was cooled to 0° C. with an ice bath, and acetyl chloride (80 mg, 0.66 mmol) was added dropped to the reaction mixture. 1 hour later, the reaction mixture was warmed to RT, and stirred overnight. Then the reaction mixture was washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to give the crude product. The crude product was purified via flash chromatography on silica gel (20% to 45% EtOAc in petroleum ether) to give 1-(4-(3-((1-(quinolin-2-yl)piperidin-4-yl)oxy)pyrazin-2-yl)piperazin-1-yl)ethanone (108 mg, 0.25 mmol, 78% yield) as a white solid. ESI-MS (M+1): 433 calc. for C24H28N6O2 432.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376450B2
Source datasetuspto-grants-2016_06
ORD IDord-b25ba489609649ae9e5b3439cfdd6a30
Source noteuspto-grants-2016_06