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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624350Generated: November 2, 2026

Diisopropylethylamine → 4-(1-Cyclopropylpiperidin-4-ylamino)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/624350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Cyclopropylpiperidin-4-amineHCID 16227644—
Reactant4-Fluoro-3-nitrobenzenesulfonamideHCID 16782487—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-(1-Cyclopropylpiperidin-4-ylamino)-3-nitrobenzenesulfonamideHCID 26042751—

Reaction Steps

To a solution of 4-fluoro-3-nitrobenzenesulfonamide (1.26 g) and 1-cyclopropylpiperidin-4-amine (0.802 g) in tetrahydrofuran (20 mL) was added N,N-diisopropylethylamine (2.22 g) and 4-dimethylaminopyridine (35 mg). The mixture was stirred at reflux overnight. The mixture was diluted with ethyl acetate (200 mL) and washed with aqueous NaHCO3, water, and brine and dried over Na2SO4. After filtration and concentration, the residue was dissolved in dichloromethane and loaded on a column and eluted with dichloromethane (500 mL), 5% 7N NH3 in 10% methanol in dichloromethane (1.5 L) to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303025B2
Source datasetuspto-grants-2016_04
ORD IDord-0355c74bd4fc4a388b179c5d8f97c0cf
Source noteuspto-grants-2016_04