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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130467Generated: October 30, 2026

HCID 55207327, compound → HCID 86616289, compound

https://huagongshe.com/reaction/130467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 55207327HCID 55207327—
Reactant5-(cis-3,5-Dimethyl-1-piperazinyl)-2-(methyloxy)anilineHCID 59007063—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 86616289HCID 86616289—

Reaction Steps

A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)aniline (D4) (587 mg, 2.5 mmol) in dichloromethane (4 ml) and pyridine (4 ml) was treated with a suspension of 6-chloro-3-pyridinesulfonyl chloride hydrochloride (D32) (700 mg, 3 mmol) in dichloromethane (4 ml). After stirring at room temperature for 15 minutes the mixture was evaporated and the residue co-evaporated with toluene (×2). The residue was then partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The organic layer was separated, washed in water, brine, dried and evaporated. The residue was triturated with ether/and dried to give the title product. MS (ES+) 411/413 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381728B2
Source datasetuspto-grants-2008_06
ORD IDord-fe994d2f90824d7792da66e3fafb757b
Source noteuspto-grants-2008_06