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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583202Generated: October 29, 2026

Pyridine → 4-phenyl-1-(N-chloroacetyl-2-methylindoline-5-sulfonyl)-2-imidazolone

https://huagongshe.com/reaction/583202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroacetyl chlorideHCID 6577—
ReactantHCID 21224941HCID 21224941—
SolventDichloromethaneHCID 6344—
Product4-phenyl-1-(N-chloroacetyl-2-methylindoline-5-sulfonyl)-2-imidazoloneHCID 2122487294%

Reaction Steps

4-Phenyl-1-(2-methylindoline-5-sulfonyl)-2-imidazolone (300 mg, 0.85 mmol) prepared in Preparation 3 was dissolved in 10 m of dichloromethane. Pyridine (75 μ, 0.93 mmol) and chloroacetylchloride (74 μ, 0.93 mmol) were added thereto one after another, and then the reaction mixture was stirred at room temperature under nitrogen atmosphere for 2 hours. After stirring, the reaction mixture was diluted with 50 m of dichloromethane, washed with water, dried over anhydrous magnesium sulfate, and then concentrated. The residue was purified by silica gel column chromatography (eluent:dichloromethane/methanol=10/1, v/v) to afford 342 mg of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929103
Source datasetuspto-grants-1999_07
ORD IDord-1c1248fd31b9462a8283dcef0b96fc2a
Source noteuspto-grants-1999_07