HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503173Generated: October 26, 2026
Water → 5-Bromo-3-(3-fluorophenyl)-7-methyl-1-trityl-1H-indazole
https://huagongshe.com/reaction/503173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Triphenylmethane chloride | HCID 22260971 | — |
| Reactant | HCID 178422425 | HCID 178422425 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-3-(3-fluorophenyl)-7-methyl-1-trityl-1H-indazole | HCID 22260740 | 42.4% |
Reaction Steps
To a solution of 2.56 g of 5-bromo-3-(3-fluorophenyl)-7-methyl-1H-indazole in 30 ml of dimethylformamide was added 0.50 g of sodium hydride at room temperature, and the mixture was stirred at the same temperature for 15 minutes. At the same temperature, 2.34 g of triphenylmethane chloride was added and the mixture was stirred at the same temperature for one day. Water was added to the reaction mixture and the mixture was diluted with ethyl acetate. The organic layer was sequentially washed with saturated aqueous ammonium chloride solution and brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=1:10) and the resulting crystals were washed with diethyl ether, to give 1.94 g of the title compound as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776890B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-88bc4aa935b647c1b7fdc95300a009ec |
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| Source note | uspto-grants-2010_08 |
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