2-(hydroxybenzyl) benzo [d] isothiazolone compound as well as preparation method and application thereof
A technology of isothiazolone and hydroxybenzyl, which is applied to 2-(hydroxybenzyl)benzo[d]isothiazolone compounds, and the fields of their preparation and use, can solve the problem of poor long-term curative effect and target of action in AD patients Single, multiple toxic and side effects
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Embodiment 1
[0039] 2-(Hydroxybenzyl) benzo [d] isothiazolone compound (I) preparation general method
[0040] Dissolve 1.0 mmol of 2-(hydroxybenzyl)benzo[d]isothiazolone compound (1) in 8 ml of ethanol, add 3.0 mmol of paraformaldehyde and the corresponding amine compound (HNR 4 R 5 ) 3.0 mmol, heated and refluxed and stirred for 2-48 hours (the reaction process was tracked by TLC), after the reaction was completed, the solvent was evaporated under reduced pressure, 50 ml of dichloromethane was added to the residue, washed with 20 ml of saturated brine, and the organic layer was After drying over anhydrous sodium sulfate and filtering, the solvent was evaporated under reduced pressure, and the residue was purified by column chromatography (eluent: petroleum ether-ethyl acetate=1:3 v / v) to obtain the corresponding 2-(hydroxybenzyl base) benzo [d] isothiazolone compound (I), the yield is 36.0%-80.5%, and its chemical structure has been verified 1 H-NMR, 13 It was confirmed by C-NMR and E...
Embodiment 2
[0064] Example 2 General method for the preparation of 2-(hydroxybenzyl)benzo[d]isothiazolone compound (I) and acid salt formation
[0065] Add 2.0 mmol of 2-(hydroxybenzyl) benzo [d] isothiazolone compound (I) obtained in Example 1 above and 30 ml of acetone into the reaction flask, stir evenly, add 7.0 mmol of the corresponding acid, and heat up The reaction was stirred under reflux for 30 minutes, cooled to room temperature after the reaction was completed, the solvent was evaporated under reduced pressure, the residue was recrystallized with acetone, and the precipitated solid was filtered to obtain 2-(hydroxybenzyl)benzo[d]isothiazolone compounds (I) salts whose chemical structures have been 1 Confirmed by H NMR and ESI-MS.
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