반응 #595350
ord-2ea36c54df0948bda397cf370e38abdd
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후처리
- 1여과The mixture is then filtered through Celite, which
- 2세척is washed with warm water
- 3기타The filtrate obtained
- 4추출extracted three times with in each case 20 ml of diethyl ether
- 5건조The combined organic phases are dried over magnesium sulfate
- 6기타the solvent is removed on a rotary evaporator
- 7기타The residue is purified by preparative HPLC (column: YMC GEL ODS-AQ S-5/15 μm; mobile phase gradient: acetonitrile/water 10:90→95:5)
실험 절차
556 mg (2.25 mmol) of the compound from Example 41A and 14.7 ml of dioxane are added to a suspension of 802 mg (4.72 mmol) of silver(I) nitrate in 2 ml of water. A solution of 193 mg (4.84 mmol) of sodium hydroxide in 7.8 ml of water is then added slowly. The mixture is stirred at RT for 3 h. The mixture is then filtered through Celite, which is washed with warm water. The filtrate obtained is acidified by addition of 1 N hydrochloric acid and extracted three times with in each case 20 ml of diethyl ether. The combined organic phases are dried over magnesium sulfate and the solvent is removed on a rotary evaporator. The residue is purified by preparative HPLC (column: YMC GEL ODS-AQ S-5/15 μm; mobile phase gradient: acetonitrile/water 10:90→95:5).