Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426037Generated: November 1, 2026

Piperazine → HCID 58707256, compound

https://huagongshe.com/reaction/2426037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4-Difluoro-1-(methylsulfonyl)benzeneHCID 2758336—
Reactant1-Benzothiophen-3-amineHCID 11194423—
ReactantHCID 67147307HCID 67147307—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 58707256HCID 5870725616%

Reaction Steps

A solution of benzo[b]thiophen-3-amine (1.1 mmol), 2,4-difluoro-1-(methylsulfonyl)benzene (1.1 mmol) and N,N-diisopropylethylamine (4.00 mmol) in N,N-dimethylformamide (2 mL) was stirred at 110° C. for 16 h. The reaction was cooled to room temperature, poured over water and extracted with diethyl ether. The solvent was concentrated in vacuo and the residue was used without further purification for the following reaction. N-(5-fluoro-2-(methylsulfonyl)phenyl)benzo[b]thiophen-3-amine (0.3 mmol), piperazine (8.0 mmol), N,N-diisopropylethylamine (4.00 mmol) were stirred at 80° C. in dry acetonitrile (3 mL) for 16 h. The solvent was evaporated and the residue was dissolved in dichloromethane and washed with water. The dichloromethane was evaporated and the crude compound was purified by silica chromatography using 10% methanol in dichloromethane to afford the title compound (16% yield). 1H NMR (400 MHz, CDCl3): δ 8.12 (s, 1H), 7.88 (m, 1H), 7.71 (d, 1H), 7.71 (m, 1H), 7.66 (m, 1H), 7.14 (s, 1H), 6.46 (d, 1H), 6.41 (dd. 1H), 3.13 (s, 3H), 3.11 (m, 4H), 2.91 (m, 4H); MS (ESI) m/z: 388.2 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968538B2
Source datasetuspto-grants-2011_06
ORD IDord-df37774a976a480d9acf95513e3e6947
Source noteuspto-grants-2011_06