Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantCesium carbonateHCID 10796—
Reactanttert-Butyl 5-bromo-1H-indazole-1-carboxylateHCID 22832025—
ReactantHCID 86620564HCID 86620564—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
Product5-(4-Fluoro-3-formylphenyl)-indazole-1-carboxylic acid tert-butyl esterHCID 8661646971.5%

Reaction Conditions

Temperature85 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618650B2
Source datasetuspto-grants-2009_11
ORD IDord-bc21cd5fa5dd467093117d3c4ed36577
Source noteuspto-grants-2009_11