744256-69-7Relevant articles and documents
Preparation method of high-purity clopidogrel
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, (2017/08/30)
The invention relates to a preparation method of high-purity clopidogrel (formula I). The preparation method comprises the following steps: firstly, performing reaction on a compound as shown in formula II and a compound as shown in formula III in an acetone solvent under the existence of alkali, filtering reactants to remove insolubles, and adding sulfuric acid into filtrate for separation and crystallization, thus obtaining clopidogrel disulfate with the optical purity of 98 percent or above; neutralizing the clopidogrel disulfate with inorganic alkali in dichloromethane and water, obtaining clopidogrel free alkali, salifying the clopidogrel free alkali and benzenesulfonic acid in an alcohol solvent, then adding an alkane solvent for separation and crystallization, thus obtaining clopidogrel benzene sulfonate (formula V) with the optical purity of 99.9 or above, and applying the clopidogrel benzene sulfonate to a medicine preparation, or neutralizing the clopidogrel disulfate with the inorganic alkali in the dichloromethane and the water, thus obtaining the clopidogrel free alkali with the optical purity of 99.9 percent, and applying the clopidogrel free alkali to preparation of pharmaceutically acceptable salt and a medicine preparation.
HIGHLY PURE SALTS OF CLOPIDOGREL FREE OF GENOTOXIC IMPURITIES
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Page/Page column 14, (2012/10/07)
The present invention relates to substantially pure salts of clopidogrel of Formula (I) substantially free from genotoxic impurities. (I) wherein (S) represents a suitable organic or inorganic acid, which forms a salt with clopidogrel having less acidity.
Pharmaceutical formulations comprising clopidogrel
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Page/Page column 5, (2008/06/13)
The formation of melt granulates comprising the drug clopidogrel of the following formula or a pharmaceutically acceptable salt thereof markedly reduces degradation of clopidogrel and its salts on storage.