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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395782Generated: October 30, 2026

Acetonitrile → HCID 21477689, compound

https://huagongshe.com/reaction/2395782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-BromopropeneHCID 11202—
Reactanttert-Butyl 4-(3-aminopyridin-2-yl)piperazine-1-carboxylateHCID 2756375—
SolventDichloromethaneHCID 6344—
SolventPotassium CarbonateHCID 11430—
ProductHCID 21477689HCID 21477689—

Reaction Steps

A mixture of 1-[1,1-dimethylethoxycarbonyl]-4-[3-amino-2-pyridinyl]piperazine (International Publication 88/08424, 2.78 g), 2-bromopropene (1.87 g), anhydrous potassium carbonate (3.3 g) and acetonitrile (100 ml) is refluxed for 36 hr. The mixture is cooled and then diluted with dichloromethane and aqueous potassium carbonate solution. The phases are separated and the organic phase is washed with saline and than concentrated in vacuo. Purification by flash column chromatography (2% methanol/chloroform) provided of the title compound. Capillary GC analysis (HP1 column, initial temperature at 100° for 1 min, then programmed to rise 20° per minute to 250°) gave a peak at 6.06 (96%) minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489593
Source datasetuspto-grants-1996_02
ORD IDord-3108745ce2594c7e8bc1483b4b178e65
Source noteuspto-grants-1996_02