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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605814Generated: November 1, 2026

Dichloromethane → HCID 67067092, compound

https://huagongshe.com/reaction/605814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 67067109HCID 67067109—
SolventChloroformHCID 6212—
ProductHCID 67067092HCID 67067092—

Reaction Steps

TEA (0.23 ml) and benzenesulfonyl chloride (0.075 ml) were added to a dichloromethane (5 ml) solution containing 3-pyridyl 1-piperazinecarboxylate dihydrochloride (150 mg), followed by stirring overnight at room temperature. The reaction solution was diluted with chloroform, the organic layer was washed with aqueous saturated sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography (eluent: chloroform), and the resulting solid was recrystallized from 2-propanol to obtain 3-pyridyl 4-(phenylsulfonyl)-1-piperazinecarboxylate (130 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915261B2
Source datasetuspto-grants-2011_03
ORD IDord-061a3ed0204d41ed80b79cc78b0705dd
Source noteuspto-grants-2011_03