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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772287Generated: October 27, 2026

Piperazine → 5-Fluoro-2-(piperazin-1-ylmethyl)-1,3-benzothiazole

https://huagongshe.com/reaction/1772287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Bromomethyl)-5-fluorobenzo[d]thiazoleHCID 14458627—
SolventAcetonitrileHCID 6342—
Product5-Fluoro-2-(piperazin-1-ylmethyl)-1,3-benzothiazoleHCID 62309456—

Reaction Steps

A mixture of 2-(bromomethyl)-5-fluoro-1,3-benzothiazole (150 mg, 0.61 mmol), potassium carbonate (253 mg, 1.83 mmol) and piperazine (263 mg, 3.05 mmol) in acetonitrile (30 ml) was heated at reflux for 4.5 hours with stirring and was then concentrated under vacuum. The residue was dissolved in dichloromethane (100 ml), washed with brine (3×50 mL), dried over anhydrous sodium sulfate, filtered and concentrated under vacuum to afford 5-fluoro-2-(piperazin-1-ylmethyl)-1,3-benzothiazole as a yellow crude solid (130 mg). (ES, m/z): [M+H]+ 252.1; 1H NMR (400 MHz, CDCl3): δ 7.81 (dd, J=8.8, 5.2 Hz, 1H), 7.70 (dd, J=9.6, 2.4 Hz, 1H), 7.16-7.11 (m, 1H), 3.93 (s, 2H), 2.97-2.93 (m, 4H), 2.64-2.63 (m, 4H), 1.98 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249102B2
Source datasetuspto-grants-2016_02
ORD IDord-33fde6eaea2f40ffa1dfe43f64403f41
Source noteuspto-grants-2016_02