2-Methyl-3-butyn-2-ol → 2-methyl-4-(3-pyridinyl)-3-butyn-2-ol

温度

0 °C

3-Bromopyridine (3.0 mL, 31 mmol), triethylamine (22 mL, 160 mmol), CuI (1.2 g, 6.2 mmol), and PdCl2(PPh3)2 (1.1 g, 1.5 mmol) were combined in DME (92 mL) and cooled to 0° C. 2-Methyl-3-butyne-2-ol (9.0 mL, 93 mmol) was then added and the reaction was allowed to slowly warm to ambient temperature. The mixture was then heated to 55-60° C. for 16 h. The mixture was filtered through Celite.™., and the pad was washed thoroughly with ethyl acetate. The combined filtrates were washed with brine (3.times.100 mL), dried over MgSO4, and filtered. The solution was concentrated in vacuo, and the residue was purified by column chromatography eluting with 90:10 hexane:ethyl acetate then ethyl acetate to afford 2-methyl-4-(3-pyridinyl-)-3-butyn-2-ol (2.0 g, 40% yield) as a brown oil 1H NMR (CDCl3, 300 MHz) Δ8.76 (br s, 1H), 8.52 (br s, 1H), 7.74-7.70 (m, 1H), 4.08 (br s, 1H), 1.63 (s, 3H). MS (EI ionization) 161 (M+).

1. temperatureto slowly warm to ambient temperature
2. temperatureThe mixture was then heated to 55-60° C. for 16 h
3. filtrationThe mixture was filtered through Celite
4. wash, and the pad was washed thoroughly with ethyl acetate
5. washThe combined filtrates were washed with brine (3.times.100 mL)
6. dry with materialdried over MgSO4
7. filtrationfiltered
8. concentrationThe solution was concentrated in vacuo
9. customthe residue was purified by column chromatography
10. washeluting with 90:10 hexane

ORDレコード

ord-fbaa0e3bd4c1489380ad1e39ddbe8ec1

出典データセット

uspto-grants-2008_12

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07462619B2