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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-phenyl-2,3-dihydro-1H-imidazol-2-one | HCID 11062677 | — |
| Reactant | 1-(Trifluoroacetyl)-2,3-dihydro-1H-indole-5-sulfonyl chloride | HCID 11088306 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-phenyl-1-(N-trifluoroacetylindoline-5-sulfonyl)-2-imidazolone | HCID 21224874 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05932742 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-4fb762a2e3904d59ab7ae167953b0f9c |
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| Source note | uspto-grants-1999_08 |
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