Toluene → 2-[[3-[(5-Methyl-2-phenyl-4-oxazolyl)methoxy]-5-isoxazolyl]methoxy]nicotinaldehyde

To a mixture of 2-[[3-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]-5-isoxazolyl]methoxy]nicotinonitrile (2.60 g) and anhydrous toluene (100 mL) was dropwise added a solution (0.95 M, 15.5 mL) of diisobutylaluminum hydride in hexane at −78° C. The reaction mixture was allowed to warm to room temperature with stirring for 1.5 hrs. A saturated aqueous ammonium chloride solution (30 mL) was dropwise added to the mixture and the mixture was further stirred at room temperature for 30 min. Ethyl acetate was added to the mixture and the mixture was washed with saturated aqueous ammonium chloride solution and then with saturated brine. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The obtained residue was subjected to silica gel column chromatography to give crystals (1.70 g, 65%) of 2-[[3-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]-5-isoxazolyl]methoxy]nicotinaldehyde from a fraction eluted with ethyl acetate-hexane (1:2, v/v). Recrystallization from ethyl acetate-hexane gave colorless needle crystals. melting point: 90-91° C.

1. stirringthe mixture was further stirred at room temperature for 30 min
2. washthe mixture was washed with saturated aqueous ammonium chloride solution
3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
4. concentrationconcentrated

ORDレコード

ord-4dbcfb3763e34f5b867392557b769c05

出典データセット

uspto-grants-2007_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07238716B2