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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554394Generated: October 25, 2026

Methanamine, hydrochloride (1:1) → 1-(5-(4-Fluorophenyl)-1-{[4-(trifluoromethyl)phenyl]sulfonyl}-1H-pyrrol-3-yl)-N-methylmethanamine

https://huagongshe.com/reaction/554394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanamine, hydrochloride (1:1)HCID 11637—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-(4-fluorophenyl)-1-{[4-(trifluoromethyl)phenyl]sulfonyl}-1H-pyrrole-3-carbaldehydeHCID 86620777—
SolventMethanolHCID 887—
Product1-(5-(4-Fluorophenyl)-1-{[4-(trifluoromethyl)phenyl]sulfonyl}-1H-pyrrol-3-yl)-N-methylmethanamineHCID 6692480868.3%

Reaction Steps

To a solution (12 mL) of 5-(4-fluorophenyl)-1-{[4-(trifluoromethyl)phenyl]sulfonyl}-1H-pyrrole-3-carbaldehyde (0.55 g) in methanol were added methylammonium chloride (1.11 g) and sodium cyanoborohydride (0.26 g), and the mixture was stirred at room temperature for 18 hr. The reaction mixture was concentrated under reduced pressure, saturated aqueous sodium hydrogen carbonate was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent: hexane-ethyl acetate=1:1) to give the title compound as colorless crystals (yield 0.39 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-5df254573bf1441db3ee8046dcefcc26
Source noteuspto-grants-2011_11