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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260255Generated: October 26, 2026

Acetic Acid → 4-isopropyl-N-[4-((S)-1-ethyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/1260255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetaldehydeHCID 177—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-Isopropyl-N-((S)-4-pyrrolidin-3-yl-phenyl)-benzenesulfonamideHCID 57470074—
SolventDichloromethaneHCID 6344—
Product4-isopropyl-N-[4-((S)-1-ethyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamideHCID 53628696—

Reaction Steps

0.3 g of 4-Isopropyl-N—((S)-4-pyrrolidin-3-yl-phenyl)-benzenesulfonamide (0.87 mmol) were dissolved in 20 ml dichloromethane. After addition of 0.07 ml of acetic acid, 0.073 ml of acetaldehyde (1.31 mmol) and 0.277 g of sodium triacetoxyborohydride (1.31 mmol), the reaction mixture was stirred at room temperature for 30 minutes. The solvent was evaporated, the residue dissolved in water and the pH adjusted to pH 8-9 with aqueous sodium hydroxide solution. The aqueous phase was extracted three times with diethyl ether, the combined organic phases dried over magnesium sulfate, filtered, and the solvent evaporated under reduced pressure. The crude product was purified via silica gel chromatography (chromabond column) with dichloromethane, dichloromethane/methanol 4% as eluent to yield 64 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470810B2
Source datasetuspto-grants-2013_06
ORD IDord-487fef36071c41208366af087cc91c6b
Source noteuspto-grants-2013_06