Diethyl Oxalate → Ethyl(3-fluoro-2-iodopyridin-4-yl)oxoacetate

温度

0 °C

n-Butyllithium (1.59M in hexane) (1.75 ml, 2.78 mmol) was added to a solution of diisopropylamine (390 μl, 2.78 mmol) in tetrahydrofuran (10 ml) at −78° C., and the mixture was warmed up to 0° C., then stirred for 30 minutes. The mixture was again cooled down to −78° C. A solution of 3-fluoro-4-iodopyridine (500 mg, 2.24 mmol) synthesized by the method of P. Rocca et. al. (Tetrahedron 49,49–64(1993)) in tetrahydrofuran (4 ml) was added to said mixture, and the resulting mixture was stirred for 1.5 hours. The reaction mixture was dropwise added to a solution of diethyl oxalate (900 μl, 6.63 mmol) in tetrahydrofuran (10 ml) at −78° C. under stirring. The mixture was warmed up to room temperature and stirred for 20 minutes. Aqueous ammonium chloride was added to the reaction mixture, and the mixture was extracted with chloroform. The extract was dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane:ethyl acetate, 3:2) to give the title compound (659 mg).

1. temperatureThe mixture was again cooled down to −78° C
2. stirringthe resulting mixture was stirred for 1.5 hours
3. stirringunder stirring
4. temperatureThe mixture was warmed up to room temperature
5. stirringstirred for 20 minutes
6. extractionthe mixture was extracted with chloroform
7. dry with materialThe extract was dried over anhydrous magnesium sulfate
8. concentrationconcentrated in vacuo
9. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate, 3:2)

ORDレコード

ord-a531a708bc834d2a8e145f86f672b44a

出典データセット

uspto-grants-2006_12

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07148224B2