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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840584Generated: November 3, 2026

Tert-butyl 3-oxopiperazine-1-carboxylate → HCID 86586605, compound

https://huagongshe.com/reaction/1840584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
ReactantHCID 23447336HCID 23447336—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductHCID 86586605HCID 8658660576.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 6-(6-chloropyrimidine-4-yl)-1-oxa-6-azaspiro[2,5]octane (4.00 g) and 4-(tert-butoxycarbonyl)-2-piperazinone (3.38 g) in tert-butylalcohol (50 ml) was added potassium tert-butoxide (0.57 g), and the mixture was stirred at 80° C. overnight. The reaction solution was concentrated, and the residue was diluted with ethyl acetate (100 ml), washed with 0.5N hydrochloric acid and saturated brine, dried and concentrated. The residue was purified with silica gel column chromatography (eluent: ethyl acetate) and crystallized from a mixture of ethyl acetate and diethylether to give colorless crystals of 4-(tert-butoxycarbonyl)-1-[1-(6-chloro-4-pyrimidinyl)-4-hydroxypiperidin-4-ylmethyl]piperazin-2-one (5.51 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680312B2
Source datasetuspto-grants-2004_01
ORD IDord-63bd9e7e9f344921a7a7db7946648363
Source noteuspto-grants-2004_01