2,6-Dimethylpyrazine → 2-[(E)-2-(3-fluorophenyl)ethenyl]-6-methylpyrazine

온도

0 °C

2,6-Dimethylpyrazine (5.0 g, 46 mmol) was dissolved in THF (200 mL) and cooled to 0° C. Potassium t-butoxide (46 mL of a 1.0M solution in THf, 46 mmol) was added to afford a dark red solution. The solution was allowed to warm to ambient temperature and stir for 1 hr. The solution was then cooled to 0° C., and 3-fluorobenzaldehyde (4.9 mL, 46 mmol) was added via syringe pump over 2 h. The reaction was then allowed to slowly warm to ambient temperature. After stirring at ambient temperature for 18 h, the reaction mixture was cooled to 0° C. and quenched by the addition of concentrated aqueous HCl (10 mL). The resulting suspension was allowed to warm to ambient temperature for 15 minutes, then cooled to 0° C. and brought to pH=8 by addition of solid NaHCO3. The layers were separated, and the aqueous layer was extracted with ethyl acetate (3.times.200 mL). The combined organic layers were washed with brine (200 mL), dried over MgSO4, filtered, and concentrated in vacuo. The crude product was purified by column chromatography eluting with 90:10, 85:15, then 80:20 hexane:ethyl acetate to afford 2-[(E)-2-(3-fluorophenyl)ethenyl]-6-methylpyrazine (4.14 g, 42% yield) as a light yellow solid. M.p. 43-44° C. 1H NMR (CDCl3, 300 MHz) Δ8.44 (s, 1H), 8.31 (s, 1H), 7.29 (d, J=16 Hz, 1H), 7.37-7.26 (m, 3H), 7.12 (d, J=16 Hz, 1H), 7.05-6.98 (m, 1H), 2.59 MS (ESI) 214.5 (M+). This material was carried on to the next step without further purification.

1. customto afford a dark red solution
2. temperatureto warm to ambient temperature
3. temperatureThe solution was then cooled to 0° C.
4. temperatureto slowly warm to ambient temperature
5. stirringAfter stirring at ambient temperature for 18 h
6. temperaturethe reaction mixture was cooled to 0° C.
7. customquenched by the addition of concentrated aqueous HCl (10 mL)
8. temperatureto warm to ambient temperature for 15 minutes
9. temperaturecooled to 0° C.
10. additionbrought to pH=8 by addition of solid NaHCO3
11. customThe layers were separated
12. extractionthe aqueous layer was extracted with ethyl acetate (3.times.200 mL)
13. washThe combined organic layers were washed with brine (200 mL)
14. dry with materialdried over MgSO4
15. filtrationfiltered
16. concentrationconcentrated in vacuo
17. customThe crude product was purified by column chromatography
18. washeluting with 90:10, 85:15

ORD 기록

ord-5e1ce91d8c9346ee84c8d69d1772f97b

출처 데이터셋

uspto-grants-2008_04

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07365074B2