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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584665Generated: November 3, 2026

Pyridine → HCID 21224938, compound

https://huagongshe.com/reaction/1584665

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 ml of dichloromethane. Pyridine (0.1 ml, 0.58 mmol) and benzoyl chloride (0.1 g, 0.58mmol) 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 ml of dichloromethane, washed twice with 10 ml 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 numberUS05932742
Source datasetuspto-grants-1999_08
ORD IDord-1a16f20a41714107b18c71b1138c5ff5
Source noteuspto-grants-1999_08