Piracetam pharmaceutical co-crystal taking 3,4-dihydroxy-benzoic acid as precursor and preparation method of piracetam pharmaceutical co-crystal
A technology of dihydroxybenzoic acid and piracetam, applied in organic chemistry and other fields, can solve the problem of ineffectiveness in patients with severe dementia, and achieve the effect of improving stability and bioavailability
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[0028] Synthesis of co-crystals using piracetam and 3,4-dihydroxybenzoic acid:
[0029] Weighing:
[0030] The reactants were fed with 20.00 mg of piracetam and 30.00 mg of 3,4-dihydroxybenzoic acid. Accurately weigh 20.00 mg of piracetam and 30.00 mg of 3,4-dihydroxybenzoic acid with an analytical balance, and add them into a transparent glass vial.
[0031] Dissolution of API:
[0032] Use a 5ml pipette to accurately measure 5ml of methanol into a 20ml transparent glass vial, and stir on a stirrer for 1h to dissolve all the solids, and the solution becomes a colorless clear liquid.
[0033] Solvent room temperature volatilization heat method:
[0034] After the solid is completely dissolved, take out the stirring bar, seal the mouth of the bottle with tinfoil, prick a few small holes with a needle, and let it stand for volatilization. After about 6 days, a colorless and transparent block crystal was precipitated in the bottle, that is, piracetam co-crystal.
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