HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489437Generated: October 31, 2026
Methanesulfonyl chloride → HCID 10674287, compound
https://huagongshe.com/reaction/1489437
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 10695920 | HCID 10695920 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10674287 | HCID 10674287 | — |
Reaction Steps
1-[(1R,2S)-2-(2,4-Difluorophenyl)-2,3-dihydroxy-1-methylpropyl]-3-[4-(1,1,2,2-tetrafluoroethoxy)phenyl]-2(1H,3H)-imidazolone (0.5 g) was dissolved in 20 ml of ethyl acetate, to which 0.12 ml of methanesulfonyl chloride and 0.22 ml of triethylamine were added dropwise with ice cooling. After stirring at 0° C. for 30 minutes, the reaction solution was washed with water (10 ml×2) and 10 ml of an aqueous solution of sodium chloride successively. The organic layer was dried over magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was purified by silica gel chromatography (silica gel: 50 g, eluent; hexane:ethyl acetate=1:1). The desired fraction was concentrated to give 0.58 g of 1-[(1R,2S)-2-(2,4-difluorophenyl)-2-hydroxy-3-methanesulfonyloxy-1-methylpropyl]-3-[4-(1,1,2,2-tetrafluoroethoxy)phenyl]-2(1H,3H)-imidazolone as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05677464 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-28586770341f4e1294b2333c5e40263f |
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| Source note | uspto-grants-1997_10 |
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