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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864404Generated: October 26, 2026

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

https://huagongshe.com/reaction/864404

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 1.44δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563142
Source datasetuspto-grants-1996_10
ORD IDord-5577ecd3e92b486691e338e2d394c783
Source noteuspto-grants-1996_10