反応 #2286336
ord-f7ee0f6ba36d46de851dc2e073e8a363
反応方程式
反応物
試薬
反応条件
後処理
- 1濃縮At this time, the reaction was concentrated in vacuo
- 2濃縮hexanes followed by concentration under vacuum
- 3workup.ADDITIONThe resulting solid was diluted with water (100 mL)
- 4workup.ADDITIONwas then treated with a 1N aqueous sodium hydroxide solution
- 5抽出This solution was extracted with ethyl acetate
- 6抽出This solution was then extracted with ethyl acetate (2×100 mL)
- 7洗浄The organics were washed with a saturated aqueous sodium chloride solution (1×100 mL)
- 8乾燥dried with magnesium sulfate
- 9ろ過filtered
- 10濃縮concentrated under vacuum
実験手順
A mixture of [3,5-dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-ylsulfanyl)-phenyl]-acetic acid (75) (90 mg, 0.23 mmol) and sodium acetate (66 mg, 0.80 mmol) in glacial acetic acid (2.5 mL) was heated to 100° C. for 7 h. At this time, the reaction was concentrated in vacuo. The residue was slurried three times in a 1:1 solution of methylene chloride:hexanes followed by concentration under vacuum. The resulting solid was diluted with water (100 mL) and was then treated with a 1N aqueous sodium hydroxide solution to adjust the pH between 10-11. This solution was extracted with ethyl acetate. The organics were discarded. The aqueous layer was then acidified to pH=2-3 with a 1N aqueous hydrochloric acid solution. This solution was then extracted with ethyl acetate (2×100 mL). The organics were washed with a saturated aqueous sodium chloride solution (1×100 mL), dried with magnesium sulfate, filtered, and concentrated under vacuum. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 70:30 hexanes/ethyl acetate with 2% glacial acetic acid) afforded [3,5-dichloro-4-(5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-ylsulfanyl)-phenyl]acetic acid (76) (41 mg, 17.5%) as a white solid; EI(+)-HRMS m/e calcd for C15H14Cl2N2O3S (M+H)+ 373.0175, found 373.0175. Exact Mass=372.0102; Molecular Weight=373.26