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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111415Generated: November 2, 2026

Dichloromethane → N-(1-methyl-piperidin-4-yl)-4-nitro-benzenesulfonamide

https://huagongshe.com/reaction/2111415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-methylpiperidineHCID 2737531—
SolventEthyl AcetateHCID 8857—
ProductN-(1-methyl-piperidin-4-yl)-4-nitro-benzenesulfonamideHCID 2277251591.1%

Reaction Steps

To a solution of 0.570 g (0.00477 mole) of 4-amino-1-methylpiperidine, 1.5 mL of ethyldiisopropylamine and 20 mL of dichloromethane at 0 degrees, was added 1.000 g (0.00451 mole) of 4-nitrobenzenesulfonyl chloride. The mixture was stirred for 1 hour and then diluted with 100 mL of ethyl acetate and washed successively twice with 20 mL of saturated sodium bicarbonate solution, twice with 20 mL of brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 1.23 g of N-(1-methyl-piperidin-4-yl)-4-nitro-benzenesulfonamide as a yellow solid. The material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517873B2
Source datasetuspto-grants-2009_04
ORD IDord-e8a11b5be3d04c02a8c6e21261e602c5
Source noteuspto-grants-2009_04