Pyridine methyl sulfinyl imidazopyridine derivative
A methyl and methoxy technology, applied in the field of medicine, can solve the problems of insufficient drug effect, slow onset time, affecting drug effect and pharmacokinetic parameters, etc.
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Embodiment 1
[0122] Example 1 Preparation of 2-mercapto-5-methoxy-imidazo[4,5-b]pyridine
[0123] Put 8.3g (60mmol) of 2,3-diamino-6-methoxypyridine into the reaction flask, add 200ml of 95% ethanol solution, then add 12.8g (80mmol) of potassium ethoxysulfonate, Heat under reflux for 4 hours, after the reaction is complete, cool to room temperature, pour the reaction solution into 200ml of ice water, stir evenly, adjust the pH to 3-4 with 4N hydrochloric acid, precipitate a solid, filter, wash with water until neutral, and vacuum-dry the filter cake to obtain Product 8.5g, yield: 78.2%.
Embodiment 2
[0124] Example 2 Preparation of 1-(4-chloro-5,6-dimethyl-N-oxypyridin-3-yl)-4-methoxy-2-butanol
[0125] Add 300ml chloroform and 73.1g (0.3mol) 1-(4-chloro-5,6-dimethylpyridin-3-yl)-4-methoxy-2-butanol to the reaction flask, cool to 0 ℃, under stirring, add 96g (0.47mol) 85% m-chloroperoxybenzoic acid in batches, continue to stir for 1 hour, then neutralize with saturated solution of sodium bicarbonate, extract with chloroform (150ml×3), extract with Dry over anhydrous sodium sulfate, filter, and distill off the solvent under reduced pressure to obtain 66.4 g of light yellow solid, yield: 85.2%.
Embodiment 3
[0126] Example 3 Preparation of 2-(2-methoxyethyl)-6,7-dimethyl-2,3-dihydrofuro[3,2-c]pyridine oxide
[0127] Under the protection of nitrogen, add 26.0g (100mmol) of 1-(4-chloro-5,6-dimethyl-N-oxide pyridin-3-yl)-4-methoxy- 2-butanol, 100ml of toluene, then add 4g of 60% NaH (mineral oil), slowly raise the temperature to reflux, keep warm and stir for 2h, evaporate the solvent under reduced pressure, add 100ml of chloroform to the residue, and wash with 1N HCl solution, saturated After washing with sodium chloride solution, 1N sodium hydroxide solution and deionized water, it was dried over anhydrous sodium sulfate and concentrated to obtain 16.1 g of the product, yield: 72.1%.
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