Novel piracetam synthetic method
A technology of piracetam and a new method, which is applied in the field of synthesizing piracetam, can solve the problems of high production cost, and achieve the effects of simple production operation, reduced production cost, and short reaction steps
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Embodiment 1
[0021] A kind of synthetic new method of piracetam, it comprises the following steps:
[0022] Add 30.0g (0.2mol) ethyl 4-chloro-n-butyrate, 24.3g (0.22mol) glycinamide hydrochloride, 21.2g (0.2mol) sodium carbonate and 300ml absolute ethanol into a three-necked flask, heat to reflux After 20 hours, cool slightly, heat filter, evaporate the solvent dehydrated alcohol under reduced pressure, and the residue is recrystallized, filtered and dried to obtain 15.9g white crystals, which are piracetam, and the yield is 55.9% (with 4- Ethyl chloro-n-butyrate, the same below).
Embodiment 2
[0024] A kind of synthetic new method of piracetam, it comprises the following steps:
[0025] Add 30.0g (0.2mol) ethyl 4-chloro-n-butyrate, 33.2g (0.3mol) glycinamide hydrochloride, 31.8g (0.3mol) sodium carbonate and 180ml absolute ethanol into a three-necked flask, heat to reflux After 25 hours, cool slightly, heat filter, and distill off the solvent absolute ethanol under reduced pressure. The residue is recrystallized, filtered and dried to obtain 16.5 g of white crystals, namely piracetam, with a yield of 58.0%.
Embodiment 3
[0027] A kind of synthetic new method of piracetam, it comprises the following steps:
[0028] Add 30.0g (0.2mol) ethyl 4-chloro-n-butyrate, 39.8g (0.36mol) glycinamide hydrochloride, 42.4g (0.4mol) potassium carbonate and 90ml absolute ethanol into a three-necked flask, heat to reflux After 30 hours, cool slightly, heat filter, evaporate the solvent of absolute ethanol under reduced pressure, recrystallize the residue, filter and dry to obtain 16.8 g of off-white crystals, namely piracetam, with a yield of 59.1%.
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