Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352801Generated: October 26, 2026

Triethylamine → 1-[(6-Chlorobenzo[b]thien-2-yl)sulfonyl]-3-ethylpiperazine

https://huagongshe.com/reaction/352801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant6-Chlorobenzo[b]thiophene-2-sulfonyl chlorideHCID 15158641—
Reactant2-Ethyl piperazine hydrochlorideHCID 22710786—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-[(6-Chlorobenzo[b]thien-2-yl)sulfonyl]-3-ethylpiperazineHCID 22709765—

Reaction Steps

To a methylene chloride solution (30 ml) of 2-ethylpiperazine hydrochloride (307 mg) was added (6-chlorobenzo[b]thien-2-yl)sulfonyl chloride (438 mg) and triethylamine (498 mg). The resulting mixture was stirred at room temperature for 26 hours. Distilled water and methylene chloride were added and the water layer was extracted three times. The organic layers were combined, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent. The residue was subjected to chromatography on a silica gel column (methanol:methylene chloride=1:20), whereby the title compound (255 mg) was obtained as a pale yellow oil. MS (FAB) m/z: 345 [(M+H)+, Cl35], 347 [(M+H)+, Cl37]. 1H-NMR (CDCl3) δ: 0.95(3H,t,J=7.8 Hz), 1.24-1.46(2H,m), 2.16(1H,t,J=10.7 Hz), 2.54(1H,dt,J=2.9,11.2 Hz), 2.65-2.75(1H,m), 2.95(1H,dt,J=2.9,11.2 Hz), 3.04-3.10(1H,m), 3.65-3.72(2H,m), 7.43(1H,dd,J=8.8,2.0 Hz), 7.75(1H,s), 7.81(1H,d,J=8.8 Hz), 7.86(1H,s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747023B1
Source datasetuspto-grants-2004_06
ORD IDord-9c199f4918ce48d193de41e6e877a036
Source noteuspto-grants-2004_06