Hydrochloric Acid → HCID 136085249, compound

Temperature

90 °C

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).

1. customThe reaction mixture was degassed with argon
2. temperatureto cool to room temperature
3. customAfter separation of the layers
4. extractionthe aqueous phase was re-extracted with ethyl acetate
5. dry with materialThe combined organic layers were dried over magnesium sulphate
6. filtrationfiltered
7. concentrationconcentrated in vacuo
8. customThe product was purified by silica gel chromatography
9. washeluting with 5-80% ethyl acetate in hexane

ORD record

ord-d9be85c6e4a5456d97338e941ac8f633

Source dataset

uspto-grants-2011_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07960563B2