HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551427Generated: October 26, 2026
Carbonate Ion → 6-Methyl-1-phenyl-N-{[2-(trifluoromethyl)-2-oxiranyl]methyl}-1H-indazol-4-amine
https://huagongshe.com/reaction/551427
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | Bismuth trichloride | HCID 24591 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2-(Trifluoromethyl)oxiran-2-yl)methyl 4-methylbenzenesulfonate | HCID 24809749 | — |
| Reactant | 6-Methyl-1-phenyl-1H-indazol-4-amine | HCID 24938059 | — |
| Catalyst | Bismuth trichloride | HCID 24591 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Methyl-1-phenyl-N-{[2-(trifluoromethyl)-2-oxiranyl]methyl}-1H-indazol-4-amine | HCID 24938055 | 698.8% |
Reaction Steps
Bismuth chloride (347 mg, 1.1 mmol) was added to a mixture of [2-(trifluoromethyl)-2-oxiranyl]methyl 4-methylbenzenesulfonate (3.41 g, 11.5 mmol) and 6-methyl-1-phenyl-1H-indazol-4-amine (2.45 g, 1.1 mmol) in dry dichloromethane (4.5 ml) and the mixture stirred at room temperature under nitrogen over the weekend. More bismuth chloride (173 mg, 0.55 mmol) and dichloromethane (0.5 ml) were then added and the mixture stirred overnight and then diluted with chloroform (50 ml) and dry tetrahydrofuran (25 ml). N,N-Diisopropylethylamine (0.38 ml, 2.2 mmol) was added followed by polymer supported carbonate resin (Fluka, ca. 3.5 mmoles carbonate/g resin, 9.4 g) and 4 A molecular sieves. After 6 hours LCMS indicated the reaction to be complete and the mixture was filtered. The filtrate was washed with water, the aqueous phase was back-extracted with dichloromethane and the combined organic phases were dried and evaporated to give crude product which was purified by silica gel chromatography using the Flashmaster II (100 g cartridge) eluting with a 0 to 100% cyclohexane:ethyl acetate gradient. Product containing fractions were combined with similar fractions from a parallel reaction (1.28 g input of Intermediate 9) to give the title compound (2.67 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947727B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-352346f53489420ea5eae9f13b334033 |
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| Source note | uspto-grants-2011_05 |
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