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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295488Generated: October 29, 2026

Triethylamine → HCID 70505000, compound

https://huagongshe.com/reaction/2295488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
ReactantBenzenesulfinyl chlorideHCID 4190003—
SolventDichloromethaneHCID 6344—
ProductHCID 70505000HCID 70505000—

Reaction Steps

To a solution of 4.90 g of 1-(2-pyridyl)piperazine in 150 ml of dichloromethane containing 4.59 ml of triethylamine is added dropwise with stirring under nitrogen a solution of 4.82 g of benzenesulfinyl chloride in 50 ml of dichloromethane. The reaction mixture is stirred for 3 hours at room temperature, diluted with 100 ml of dichloromethane, and washed with 150 ml water and 100 ml 5% potassium carbonate. The organic layer is dried over sodium sulfate and evaporated in vacuo to give a yellow crystalline solid. Recrystallization from ethanol affords 4.14 g of 1-(2-pyridyl)piperazine-4-benzenesulfinamide as a colorless crystalline solid, mp 83°-86° (soften 81°). A second crop (1.24 g) is obtained by concentration of the mother liquors, total yield: 5.38 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04425342
Source datasetuspto-grants-1984_01
ORD IDord-5e181d8ac2d640989759296c90997302
Source noteuspto-grants-1984_01