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| Sodium carbonate (15.0 mg, 0.142 mmol, 1.1 equiv) was added to a suspension of digoxin (99.8 mg, 0.128 mmol, 1.0 equiv) and salicylaldehyde (77.81 ¦ÌL, 0.639 mmol, 5.0 equiv) in methanol (5.1 mL, 25 mM), at which point the contents turned yellow in color. A reflux condenser was affixed to the flask and the contents were warmed to reflux in a 125 ¡ãC oil bath. The reaction was cooled to room temperature after 23 h and concentrated in vacuo. The crude material was dry-loaded onto Celite and purified by flash chromatography on silica gel (1:0 ¡ú 19:1 ethyl acetate/methanol) to afford Dig(sal) (30.3 mg, 0.0342 mmol, 27% yield) as a pale yellow solid in ~8:1 dr. Mixed fractions containing the desired compounds were repurified by flash chromatography on silica gel (1:0 ¡ú 19:1 ¡ú 9:1 dichloromethane/methanol) to yield an additional 30.1 mg (0.0340 mmol, 27% yield) of Dig(sal) in ~3:1 dr. In some cases, different batches of Dig(sal) displayed varying toxicity with human embryonic kidney (HEK) 293t cells , presumably due to minor contamination with digoxin or a digoxin-related compound. Material obtained from the conditions described above can be further purified by preparative thin -layer chromatography, developing the plate thrice with either 9:1 dichloromethane/methanol or 19:1 ethyl acetate/methanol, to afford pure Dig(sal) that does not exhibit cytotoxicity up to 16 ¦ÌM with HEK 293t cell . |
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