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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934375Generated: October 31, 2026

Potassium Carbonate → HCID 86758047, compound

https://huagongshe.com/reaction/1934375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 15550445HCID 15550445—
SolventDichloromethaneHCID 6344—
ProductHCID 86758047HCID 8675804769.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of Compound B (700 mg, 2.0 mmol) in anhydrous dichloromethane (50 ml) under nitrogen at 0° C., was added 3-chloroperoxybenzoic acid (666 mg, 2.2 mmol) slowly. The resulting solution was allowed to stir for 2 hours at 0° C. and for 0.5 hour at room temperature. To the resulting clear solution potassium carbonate (415 mg, 3.0 mmol) was added, and the reaction mixture was stirred for 0.75 hour. The white precipitate was removed by filtration. The crude product was purified by flash silica gel chromatography (MeOH-CH2Cl2, 10:90 v/v containing 1% NH4OH). After drying, 505 mg of 2-(4-fluorophenyl)-5-(N-ethylpiperidin-4-yl)-3-(4-pyridyl)pyrrole N-oxide was obtained. NMR (CD3OD)σ8.26(d, J=6.27 Hz, 2H), 7.35(m, 2H), 7.26(d, J=6.13 Hz, 2H), 7.11(m, 2H), 6.28(s, 1H), 3.35(m, 6H), 2.85(m, 1H), 2.46(m, 2H), 2.00(m, 2H), 1.39(t, J=7.10 Hz, 3H); MS(ESI)=366.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384052B1
Source datasetuspto-grants-2002_05
ORD IDord-adc403f77d60415192e6336ae7c4bc67
Source noteuspto-grants-2002_05