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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583204Generated: October 29, 2026

Pyridine → HCID 21224938, compound

https://huagongshe.com/reaction/583204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 21224873HCID 21224873—
SolventDichloromethaneHCID 6344—
ProductHCID 21224938HCID 2122493892%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Phenyl-1-(indoline-5-sulfonyl)-4,5-dihydro-2-imidazolone (0.20 g, 0.58 mmol) prepared in Preparation 5 was dissolved in 12 m of dichloromethane. Pyridine (0.1 m, 0.58 mmol) and benzoyl chloride (0.1 g, 0.58 mmol) were added dropwise one after another at 0° C. under nitrogen atmosphere. The reaction mixture was stirred at 0° C. for 2 hours and further stirred at room temperature for 3 hours. The reaction mixture was diluted with 20 m of dichloromethane, washed twice with 10 m of water, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: ethylacetate/hexane=2/1, v/v) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929103
Source datasetuspto-grants-1999_07
ORD IDord-419a2dfc2dde450aa274ed40a6c449a3
Source noteuspto-grants-1999_07