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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583200Generated: October 29, 2026

Pyridine → HCID 21224903, compound

https://huagongshe.com/reaction/583200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantHCID 11002343HCID 11002343—
SolventDichloromethaneHCID 6344—
ProductHCID 21224903HCID 2122490392.7%

Reaction Steps

4-Phenyl-1-(indoline-5 -sulfonyl)-2-imidazolone (300 mg, 0.88 mmol) prepared in Preparation 3 was suspended in 10 m of dichloromethane. Then, pyridine (85 μ, 1.05 mmol) and 4-nitrobenzoyl chloride (163 mg, 0.88 mmol) were added thereto one after another. The resulting reaction mixture was stirred at room temperature under nitrogen atmosphere for 5 hours while the reaction being monitored by TLC. After the reaction was completed, the whole mixture was diluted with dichloromethane, washed with brine, dried over anhydrous magnesium sulfate, concentrated, and finally purified by silica gel column chromatography (eluent: dichloromethane/methanol=15/1, v/v) to afford 400 mg of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929103
Source datasetuspto-grants-1999_07
ORD IDord-06c5b1d6592441058d70d767f42b39d1
Source noteuspto-grants-1999_07