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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172203Generated: October 31, 2026

tert-Butyl piperazine-1-carboxylate → HCID 70873435, compound

https://huagongshe.com/reaction/2172203

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86709380HCID 86709380—
ProductHCID 70873435HCID 70873435—

Reaction Steps

2-Chloro-6-(tetrahydropyran-2-yloxy)quinoline (1.00 g) and piperazine-1-carboxylic acid tert-butyl ester (0.76 g) were heated to 140° C. in the absence of solvent under an argon atmosphere and stirred for 2 hours. After cooling the reaction mixture to room temperature, a sodium hydrogen carbonate aqueous solution was added thereto, followed by extraction with dichloromethane. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over magnesium sulfate. The result was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=75:25→67:33). The result was concentrated to dryness under reduced pressure to afford the title compound as a pale yellow amorphous compound (0.55 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051333B2
Source datasetuspto-grants-2015_06
ORD IDord-879158e30760435d8ea41b4f593e0f74
Source noteuspto-grants-2015_06