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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972665Generated: October 31, 2026

Dichloromethane → 3-((6-Methoxy-2-pyridinyl)methyl)-1-(2-thiophenylsulfonyl)piperazine

https://huagongshe.com/reaction/1972665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant2-Thiophenesulfonyl chlorideHCID 85518—
Reactant2-((6-Methoxy-2-pyridinyl)methyl)piperazineHCID 66582620—
SolventSodium BicarbonateHCID 516892—
Product3-((6-Methoxy-2-pyridinyl)methyl)-1-(2-thiophenylsulfonyl)piperazineHCID 66583382—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 100-mL round-bottomed flask were added 2-((6-methoxy-2-pyridinyl)methyl)piperazine (373 mg, 1.80 mmol), triethylamine (0.375 mL, 2.70 mmol), 2-thiophenesulfonyl chloride (0.328 mL, 1.80 mmol, Aldrich, St. Louis, Mo., and 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 light-yellow oil. The crude product was purified by silica gel chromatography, eluting with 10% MeOH/EtOAc to give 3-((6-methoxy-2-pyridinyl)methyl)-1-(2-thiophenylsulfonyl)piperazine (135 mg) as viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-9c5554b45769456389d4224c3896c285
Source noteuspto-grants-2013_04