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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584656Generated: October 31, 2026

Water → 4-phenyl-1-(N-trifluoroacetylindoline-5-sulfonyl)-2-imidazolone

https://huagongshe.com/reaction/1584656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-phenyl-2,3-dihydro-1H-imidazol-2-oneHCID 11062677—
Reactant1-(Trifluoroacetyl)-2,3-dihydro-1H-indole-5-sulfonyl chlorideHCID 11088306—
SolventDimethylformamideHCID 6228—
Product4-phenyl-1-(N-trifluoroacetylindoline-5-sulfonyl)-2-imidazoloneHCID 2122487470%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Phenyl-2,3-dihydro-1H-2-imidazolone (4 g, 24.84 mmol) prepared in Preparation 1 was suspended in 30 ml of dimethylformamide and cooled down to 0 ° C. After sodium hydride (60% oily, 1.09 g, 27.3 mmol) was added thereto, the resulting mixture was stirred for a few minutes at 0° C. until it became a clear solution. To the reaction mixture was added portionwise at 0° C. the N-trifluoroacetyl-indoline-5-sulfonylchloride (8.56 g, 27.32 mmol) prepared in Preparation 2. The reaction mixture was stirred at room temperature for 4 hours, cooled down again to 0° C., and then water was slowly added to the mixture until precipitate was formed. The resulting precipitate was collected, washed with water, and dried to afford 7.6 g of 4-phenyl-1-(N-trifluoroacetylindoline-5-sulfonyl)-2-imidazolone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05932742
Source datasetuspto-grants-1999_08
ORD IDord-4fb762a2e3904d59ab7ae167953b0f9c
Source noteuspto-grants-1999_08