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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29049Generated: October 24, 2026

p-Toluenesulfonic acid → 4-(2-(4-Fluorophenyl)-1H-pyrrol-1-yl)-N-methylbenzenesulfonamide

https://huagongshe.com/en/reaction/29049

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-amino-N-methylbenzene-1-sulfonamideHCID 74368—
Reactant3-(5,5-Dimethyl-1,3-dioxan-2-yl)-1-(4-fluorophenyl)propan-1-oneHCID 10635463—
SolventTolueneHCID 1140—
Product4-(2-(4-Fluorophenyl)-1H-pyrrol-1-yl)-N-methylbenzenesulfonamideHCID 1052044740%

Reaction Steps

A mixture of 3-(5,5-dimethyl-1,3-dioxan-2-yl)-1-(4-fluorophenyl)propan-1-one (Step 4) (400 mg, 1.5 mmol), 4-[(N-methylamino)sulfonyl]aniline (Step 6) (308 mg, 1.65 mmol) and p-toluenesulfonic acid (40 mg) in toluene (80 ml) was heated to reflux for 48 hr. The reaction mixture was cooled, filtered and concentrated. The crude yellowish solid (760 mg) was chromatographed (silica gel, hexane/ethyl acetate 7/3) to give 4-[2-(4-fluorophenyl)-1H-pyrrol-1-yl]-N-methylbenzenesulfonamide (198 mg, 40%) as a white solid: mp (DSC) 174° C. Anal Calc'd. for C17H15N2FO2S 0.25 H2O: C, 60.97; H, 4.67; N, 8.37. Found: C, 60.86; H, 4.56; N, 8.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420061B2
Source datasetuspto-grants-2008_09
ORD IDord-e856ec518eca4dabaf48ed51495e8a8b
Source noteuspto-grants-2008_09