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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972692Generated: November 4, 2026

Triethylamine → 3-(1-Propyn-1-yl)-1-(2-thiophenylsulfonyl)piperazine

https://huagongshe.com/reaction/1972692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
Reactant2-PropynylpiperazineHCID 66583809—
Reactant2-(1-Propyn-1-yl)piperazine bis(trifluoroacetate)HCID 86670441—
SolventDichloromethaneHCID 6344—
Product3-(1-Propyn-1-yl)-1-(2-thiophenylsulfonyl)piperazineHCID 66584007—

Reaction Conditions

Temperature0 °C

Reaction Steps

The 2-(1-propyn-1-yl)piperazine bis(trifluoroacetate (110 mg, 0.312 mmol) was dissolved in CH2Cl2 in a 50 mL round-bottomed flask and was then cooled to 0° C. To this solution was added an excess of triethylamine (152 μL, 1.093 mmol) followed by thiophene-2-sulfonyl chloride (57.0 mg, 0.312 mmol, Sigma-Aldrich, St. Louis, Mo.). The mixture was warmed slowly to room temperature and stirred for 2 h. Afterwards, the mixture was concentrated and absorbed onto silica gel. The crude material was purified via column chromatography (about 40 g silica gel, 0% to 10% MeOH in CH2Cl2) to give 3-(1-propyn-1-yl)-1-(2-thiophenylsulfonyl)piperazine (42 mg) as a foamy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-68114e47dbb64e71a46f68c3ddfdc81d
Source noteuspto-grants-2013_04