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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045083Generated: October 30, 2026

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

https://huagongshe.com/reaction/2045083

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 numberUS08586754B2
Source datasetuspto-grants-2013_11
ORD IDord-f1fce9c42fd54f3b8f2b393b1f456bdb
Source noteuspto-grants-2013_11