HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435558Generated: October 31, 2026
Water → 5-(4-Fluoro-3-formylphenyl)-indazole-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1435558
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | tert-Butyl 5-bromo-1H-indazole-1-carboxylate | HCID 22832025 | — |
| Reactant | HCID 86620564 | HCID 86620564 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(4-Fluoro-3-formylphenyl)-indazole-1-carboxylic acid tert-butyl ester | HCID 86616469 | 71.5% |
Reaction Steps
A mixture of 5-bromo-indazole-1-carboxylic acid tert-butyl ester (3.37 mmol), 2-fluoro-4-(4,4,5,5-tetramethyl-[1,3] dioxolan-2-yl)-benzaldehyde (1.01 g, 4.04 mmol)) PdCl2(dppf).DCM (27 mg, 0.03 mmol) in 16 mL of dioxane was degassed (evacuate in vacuo and pressurize with argon, three times); cesium carbonate in water (2M, 6.73 mL, 13.46 mmol) was added and the mixture degassed three more times as described above. The resulting mixture was heated at 85° C. for 6 h, then it was allowed to cool to room temperature and left overnight. The mixture was diluted with dichloromethane and washed with brine. The aqueous phase was extracted with dichloromethane and the combined organic phases were washed with brine, dried over MgSO4, filtered and evaporated to give crude product. Chromatography on silica gel (elution with diethyl ether/heptane) gave 820 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618650B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-bc21cd5fa5dd467093117d3c4ed36577 |
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| Source note | uspto-grants-2009_11 |
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