Nitromethane → 2-(4-Fluoro-phenoxy)-5-(2-nitro-ethyl)-pyridine

温度

100 °C

To a mixture of 6-(4-fluoro-phenoxy)-pyridine-3-carbaldehyde (150 mg, 0.69 mmol) described in Manufacturing Example 75-1-2 and acetic acid (2 mL) were added nitromethane (0.28 mL, 5.2 mmol) and ammonium acetate (160 mg, 2.1 mmol), which was stirred for 3 hours at 100° C. The reaction mixture was cooled to room temperature and water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate, and was concentrated under a reduced pressure. A mixture of dimethyl sulfoxide (3 mL) and acetic acid (0.2 mL) was added to the resulting residue, and sodium borohydride (42 mg, 1.1 mmol) was added at room temperature while cooling appropriately. The reaction mixture was stirred for 10 minutes at that temperature. Water was added at room temperature to the reaction solution at room temperature, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, and was concentrated under a reduced pressure. The residue was purified by NH silica gel column chromatography (heptane:ethyl acetate=1:1) to obtain the title compound (130 mg, 70%).

1. temperatureThe reaction mixture was cooled to room temperature
2. extractionfollowed by extraction with ethyl acetate
3. washThe organic layer was washed with saturated aqueous sodium chloride
4. dry with materialdried over anhydrous magnesium sulfate
5. concentrationwas concentrated under a reduced pressure
6. additionA mixture of dimethyl sulfoxide (3 mL) and acetic acid (0.2 mL)
7. additionwas added at room temperature
8. temperaturewhile cooling appropriately
9. stirringThe reaction mixture was stirred for 10 minutes at that temperature
10. extractionwhich was then extracted with ethyl acetate
11. washThe organic layer was washed with saturated aqueous sodium chloride
12. concentrationwas concentrated under a reduced pressure
13. customThe residue was purified by NH silica gel column chromatography (heptane:ethyl acetate=1:1)

ORDレコード

ord-9ef8b85378af42ab882190606f5ff0b4

出典データセット

uspto-grants-2012_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08158657B2