Dimethylformamide → tert-Butyl 6-benzyloxy-3-[4-cyclopropyl-5-[3-(2,2-dimethylpropyl)cyclobutyl]isoxazol-3-yl]hexanoate

Temperatur

80 °C

tert-Butyl 6-benzyloxy-3-{5-[3-(2,2-dimethylpropyl)cyclobutyl]-4-iodoisoxazole-3-yl}hexanoate (4.20 g), 2-cyclopropyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (2.34 g), tripotassium phosphate (5.92 g), DMF (90 mL) and water (10 mL) were mixed. The mixture was degassed by bubbling argon gas. To the mixture was added PdCl2(PPh3)2 (734 mg). The mixture was stirred at 80° C. for 1 hr. To the reaction mixture was added ethyl acetate, and then the mixture was filtered. The aqueous layer was removed, and the organic layer was washed with water and brine, then dried over magnesium sulfate. The magnesium sulfate was filtered off and the filtrate was concentrated in vacuo. The resultant residue was purified by silica gel column chromatography (Eluent: ethyl acetate/hexane=1/25) to give the title compound (980 mg). A mixture of the title compound and impurities thereof (1.24 g) was also obtained.

1. customThe mixture was degassed
2. customby bubbling argon gas
3. additionTo the mixture was added PdCl2(PPh3)2 (734 mg)
4. additionTo the reaction mixture was added ethyl acetate
5. filtrationthe mixture was filtered
6. customThe aqueous layer was removed
7. washthe organic layer was washed with water and brine
8. dry with materialdried over magnesium sulfate
9. filtrationThe magnesium sulfate was filtered off
10. concentrationthe filtrate was concentrated in vacuo
11. customThe resultant residue was purified by silica gel column chromatography (Eluent: ethyl acetate/hexane=1/25)

ORD-Eintrag

ord-09620ebcc6164479a0d7bf5b6167a5e7

Quelldatensatz

uspto-grants-2013_12

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08604069B2