Hydrochloric Acid → 6-[2-(4-ethoxyphenyl)ethyl]furo[3,2-c]pyridin-4(5H)-one

Temperatur

-20 °C

To a solution of 2,2,6,6-tetramethylpiperidine (11.6 mL, 68.8 mmol) in THF (100 mL) was added 1.6 M n-butyllithium hexane solution (39.0 mL, 62.4 mmol) at −78° C., and the mixture was warmed to −20° C. and stirred at the same temperature for 10 min. To this solution was added a solution of N,N-diethyl-2-methylfuran-3-carboxamide (11.3 g, 62.5 mmol) in THF (10 mL), and the mixture was further stirred for 1 hr. To the solution was added 3-(4-ethoxyphenyl)propanenitrile (11.5 g, 65.6 mmol), and the mixture was stirred at room temperature for hr. 6N Hydrochloric acid was added thereto and the mixture was extracted twice with ethyl acetate. The combined organic layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The obtained solid was washed with ethyl acetate to give the title compound (2.74 g, yield 15%) as a white solid.

1. stirringthe mixture was further stirred for 1 hr
2. stirringthe mixture was stirred at room temperature for hr
3. extractionthe mixture was extracted twice with ethyl acetate
4. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
5. customthe solvent was evaporated under reduced pressure
6. washThe obtained solid was washed with ethyl acetate

ORD-Eintrag

ord-0b917ca3b13d4b3db31464846ba24bdc

Quelldatensatz

uspto-grants-2013_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08501804B2