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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395758Generated: November 3, 2026

1,4-Dibromobutane → 1-[1,1-Dimethylethoxycarbonyl]-4-[3-(1-pyrrolidinyl)-2-pyridinyl]piperazine

https://huagongshe.com/reaction/2395758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DibromobutaneHCID 21508—
Reactanttert-Butyl 4-(3-aminopyridin-2-yl)piperazine-1-carboxylateHCID 2756375—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-[1,1-Dimethylethoxycarbonyl]-4-[3-(1-pyrrolidinyl)-2-pyridinyl]piperazineHCID 21477634—

Reaction Steps

1-[1,1-Dimethylethoxycarbonyl]-4-[3-amino-2-pyridinyl]piperazine (International Publication No. WO 88/08424, 0.50 g), 1,4-dibromobutane (0.21 ml) and potassium carbonate (0.30 g) are refluxed in 4 ml of acetonitrile for 1 week. After 1 week, additional dibromobutane (0.21 ml) is added and refluxing is continued for 3 days. The reaction mixture is poured into water, extracted with methylene chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrate is purified by flash chromatography eluting with ethyl acetate/hexane (10/90) to ethyl acetate/hexane (25/75). The appropriate fractions are pooled and concentrated to give the title compound, NMR (300 MHz, CDCl3) 7.78, 6.98, 6.78, 3.52, 3.20-3.10, 1.87 and 1.44 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489593
Source datasetuspto-grants-1996_02
ORD IDord-b7d0b789cd6e425698d1711bfb86effe
Source noteuspto-grants-1996_02