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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423068Generated: November 2, 2026

Hydrochloric Acid → HCID 136085249, compound

https://huagongshe.com/reaction/2423068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 59272968HCID 59272968—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystDi-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 136085249HCID 13608524983.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4-bromo-6-fluoro-1-{3-fluoro-4-[(phenylmethyl)oxy]phenyl}-1H-indazole (D7) (670 mg, 1.61 mmol) in dioxane (20 mL) and water (20 mL) was added potassium hydroxide (362 mg, 6.46 mmol). The reaction mixture was degassed with argon and then treated with bis(1,1-dimethylethyl)[2′,4′,6′-tris(1-methylethyl)-2-biphenylyl]phosphane (41 mg, 0.097 mmol) and tris(dibenzylideneacetone)dipalladium (0) (30 mg, 0.033 mmol). After heating at 90° C. for 1 hour, the mixture was allowed to cool to room temperature and then diluted with ethyl acetate and water. The pH was adjusted to 7 by the addition of 1M hydrochloric acid. After separation of the layers, the aqueous phase was re-extracted with ethyl acetate. The combined organic layers were dried over magnesium sulphate, filtered and concentrated in vacuo. The product was purified by silica gel chromatography eluting with 5-80% ethyl acetate in hexane to yield the title compound (D8) (473 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960563B2
Source datasetuspto-grants-2011_06
ORD IDord-d9be85c6e4a5456d97338e941ac8f633
Source noteuspto-grants-2011_06