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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840579Generated: November 2, 2026

Tert-butyl 3-oxopiperazine-1-carboxylate → HCID 23447455, compound

https://huagongshe.com/reaction/1840579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantMethyl 3-(1-benzyloxycarbonylpiperidin-4-yl)acrylateHCID 53742494—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 23447455HCID 2344745559.9%

Reaction Steps

To a solution of methyl 3-(1-benzyloxycarbonylpiperidin-4-yl)acrylate (5.55 g) and 4-(tert-butoxycarbonyl)-2-piperazinone (3.66 g) in tetrahydrofuran (50 ml) was added potassium tert-butoxide (0.56 g), and the mixture was stirred under nitrogen atmosphere at room temperature for 3 days. The reaction solution was diluted with ethyl acetate (50 ml), washed with 0.5N hydrochloric acid and saturated brine, dried and concentrated, and the residue was purified with silica gel column chromatography (eluent:acetone/hexane=1/2) to give colorless amorphous of methyl 3-(1-benzyloxycarbonylpiperidin-4-yl)-3-[4-(tert-butoxycarbonyl)-2-oxopiperazine-1-yl]propionate (5.51 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680312B2
Source datasetuspto-grants-2004_01
ORD IDord-d9ebbab093df4ab18a6773fb0372a45b
Source noteuspto-grants-2004_01