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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423071Generated: November 1, 2026

Potassium Hydroxide → HCID 136085248, compound

https://huagongshe.com/reaction/2423071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantDi-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
ReactantHCID 59272970HCID 59272970—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 136085248HCID 13608524817.1%

Reaction Steps

A solution of 4-bromo-6-chloro-1-{3-fluoro-4-[(phenylmethyl)oxy]phenyl}-1H-indazole (D10) (410 mg, 0.95 mmol) and KOH (212 mg, 3.8 mmol) in dioxane (10 mL) and water (10 mL) was sonicated under a flow of argon for 5 minutes after which the bis(1,1-dimethylethyl)[2′,4′,6′-tris(1-methylethyl)-2-biphenylyl]phosphane (24 mg, 0.057 mmol) and Pd2 dba3 (17 mg, 0.019 mmol) were added and it was heated to reflux for 2 hours. The mixture was then cooled to room temperature, diluted with EtOAc and water and the pH was adjusted to circa 7. The phases were separated, the aqueous re-extracted with EtOAc and the combined organics were finally dried over MgSO4. The crude material (450 mg) was purified by flash chromatography (Biotage SP4, 25+M silica column) with a gradient of EtOAc 0 to 50% in hexane to afford 60 mg of desired compound (D11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960563B2
Source datasetuspto-grants-2011_06
ORD IDord-b8719481f2954d40b58038e9b69c32c0
Source noteuspto-grants-2011_06