反応 #835904
ord-9b839f7882224ddb80414fb3848caab4
反応方程式
反応物
試薬
反応条件
後処理
- 1その他At −78° C.
- 2その他was gradually elevated to room temperature, at which
- 3workup.STIRRINGstirring
- 4workup.WAITwas performed for 15 hours
- 5抽出followed by extraction with ethyl acetate
- 6洗浄The organic layer was washed with brine
- 7乾燥dried over anhydrous sodium sulfate
- 8ろ過After filtration
- 9濃縮the filtrate was concentrated under reduced pressure
- 10その他the fraction obtained from the 15% ethyl acetate/hexane eluate
- 11濃縮was concentrated under reduced pressure
- 12その他The residue thus obtained
- 13その他was purified by high performance liquid chromatography (
実験手順
At −78° C., butyl lithium (a 1.57M hexane solution; 0.66 ml, 1.03 mmol) was added dropwise to a dimethoxyethane (5 ml) solution of the 2-chloro-3-(4-chlorophenylsulfonylmethyl)pyridine (156 mg, 0.516 mmol) obtained in Example 98. At −78° C., the resulting mixture was stirred for 20 minutes, followed by the addition of 1,5-diiodopentane (0.092 ml, 0.619 mmol). The temperature of the reaction mixture was gradually elevated to room temperature, at which stirring was performed for 15 hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was subjected to flash chromatography on a silica gel column, and the fraction obtained from the 15% ethyl acetate/hexane eluate was concentrated under reduced pressure. The residue thus obtained was purified by high performance liquid chromatography (using a mixed solvent of water/acetonitrile/formic acid) to give the title compound (72 mg, 38%) as a white solid. The resulting solid was washed with hexane-ether and then collected by filtration, whereby the title compound was obtained as a white powder.