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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600209Generated: October 29, 2026

Piperazine → HCID 43344301, compound

https://huagongshe.com/reaction/600209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTriethylamineHCID 8471—
Reactant5-Fluoro-2-methylbenzenesulphonyl chlorideHCID 136286—
SolventDiethyl EtherHCID 3283—
ProductHCID 43344301HCID 4334430171.1%

Reaction Steps

5-Fluoro-2-methylbenzenesulfonyl chloride (35.1 g, 168.5 mmol) in diethyl ether (50 mL) was added drop-wise to a suspension of piperazine (28.8 g, 337.0 mmol) in diethyl ether (500 mL) and triethylamine (47 mL, 337.0 mmol). The white suspension was stirred at room temp for 1.5 h. The mixture was washed with saturated aqueous sodium carbonate. The organic phase was washed with water and brine and dried (Na2SO4). Concentration gave a white solid that was triturated with diethyl ether to give the title compound as a white solid (30.95 g, 36% yield). 1H NMR (300 MHz, CDCl3) δ: 7.57 (1H, dd, J=8.6, 2.7 Hz), 7.25 (1H, dd, J=8.4, 5.1 Hz), 7.12 (1H, td, J=8.1, 2.8 Hz), 3.13-3.10 (4H, m), 2.98-2.85 (4H, m), 2.55 (3H, s), 1.69 (1H, bs). LCMS (M+H) calcd for C11H16FN2O2S: 259.09; found: 259.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902182B2
Source datasetuspto-grants-2011_03
ORD IDord-7652baa5bc9a46c2a655d68797bc641f
Source noteuspto-grants-2011_03