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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734986Generated: October 30, 2026

Dimethylamine → N,N-dimethylpiperidine-4-sulfonamide

https://huagongshe.com/reaction/734986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantBenzyl 4-(chlorosulfonyl)piperidine-1-carboxylateHCID 21931260—
SolventDimethylformamideHCID 6228—
ProductN,N-dimethylpiperidine-4-sulfonamideHCID 46779214133.3%

Reaction Steps

A suspension of an amine such as dimethylamine (4.72 mmol) and sodium hydride (4.72 mmol) in N,N-dimethylformamide (10 ml) was stirred for five minutes at room temperature. Then phenylmethyl 4-(chlorosulfonyl)-1-piperidinecarboxylate (1.60 mmol) was added to the reaction mixture and stirred at 100° C. for 3 hours. The reaction mixture was poured into water (25 ml) and extracted with ethyl acetate (3×25 ml). The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated to give the title compound (410 mg, 80% yield) as an off-white solid. MS(ES)+ m/e 327.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592342B2
Source datasetuspto-grants-2009_09
ORD IDord-26b17b507f674f7b811e61d47f6ef344
Source noteuspto-grants-2009_09