Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293745Generated: October 26, 2026

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

https://huagongshe.com/reaction/2293745

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 column 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 numberUS05686610
Source datasetuspto-grants-1997_11
ORD IDord-9703f3b50503479cae7fe52de20ae849
Source noteuspto-grants-1997_11