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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972658Generated: November 4, 2026

Triethylamine → 3-((2-Methoxy-3-pyridinyl)methyl)-1-(2-thiophenylsulfonyl)piperazine

https://huagongshe.com/reaction/1972658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
Reactant2-((2-Methoxy-3-pyridinyl)methyl)piperazineHCID 66582930—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product3-((2-Methoxy-3-pyridinyl)methyl)-1-(2-thiophenylsulfonyl)piperazineHCID 6658320233.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 100-mL round-bottomed flask was added 2-((2-methoxy-3-pyridinyl)methyl)piperazine (350 mg, 1.69 mmol), triethylamine (0.353 mL, 2.54 mmol), and 2-thiophenesulfonyl chloride (0.34 mL, 1.86 mmol, Aldrich, St. Louis, Mo.) in DCM (5 mL). The reaction mixture was stirred at 0° C. for 1 h. The reaction mixture was diluted with saturated NaHCO3 (5 mL) and extracted with EtOAc (2×30 mL). The organic extract was washed with saturated NaCl (5 mL) and dried over Na2SO4. The solution was filtered and concentrated in vacuo to give the crude material as a yellow glass. The crude product was purified by silica gel chromatography, eluting with 10% MeOH/EtOAc to give 3-((2-methoxy-3-pyridinyl)methyl)-1-(2-thiophenylsulfonyl)piperazine (202 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-7648458c42374fd9a7491d058b85f988
Source noteuspto-grants-2013_04