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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831832Generated: October 30, 2026

N-Benzylnormechlorethamine → N-(Phenylmethyl)-1-piperidinesulfonamide

https://huagongshe.com/reaction/1831832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BenzylnormechlorethamineHCID 5928—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
ReactantHCID 178486263HCID 178486263—
ProductN-(Phenylmethyl)-1-piperidinesulfonamideHCID 298959452%

Reaction Steps

To a solution of the methylene sulfonamide from part F (20.46 g, 51.5 mmol) in dimethylformamide (90 mL) was added potassium carbonate (21.3 g, 154.7 mmol), bis-(2-chloroethyl)benzyl amine (12.0 g, 51.5 mmol; and 18-Crown-6 (700 mg). The slurry was stirred at sixty degrees Celsius. After twenty four hours the reaction was concentrated in vacuo. The residue was taken up in ethyl acetate, washed with water three times, saturated sodium chloride solution, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was recrystallized (methanol) to give the N-benzyl piperidine sulfonamide as a white solid (15 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067670B2
Source datasetuspto-grants-2006_06
ORD IDord-e1c944bf8a28454b8e0dcfe276dcea89
Source noteuspto-grants-2006_06