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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518882Generated: November 4, 2026

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

https://huagongshe.com/reaction/1518882

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—
SolventSodium BicarbonateHCID 516892—
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 heated at reflux for 18 hours and upon cooling was diluted with ethyl acetate (200 mL) and aqueous NaHCO3. The crude product was isolated by concentration of the organic layer and was purified on silica gel, which was eluted with 5% methanolic ammonia in methylene chloride to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09072748B2
Source datasetuspto-grants-2015_07
ORD IDord-167f9b77ef634ceeb2d26382c9df0a3e
Source noteuspto-grants-2015_07