http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1636185-A1

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filingDate 2004-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20b62db65fcd631b7e6a60bd8739722c
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publicationDate 2006-03-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1636185-A1
titleOfInvention Novel crystalline forms of perindopril erbumine
abstract Disclosed are two novel crystalline forms d and e of perindopril erbumine, which are suitable as therapeutic substances in medicaments used for treating cardiovascular diseases, especially high blood pressure and cardiac insufficiency. Crystalline form e is obtained by crystallizing perindopril erbumine from MTBE containing 1.5 to 2.5 percent (v/v) of water at 30 to 45 DEG C, preferably 34 to 45 DEG C, crystallization expediently taking place by stirring. Crystalline form e changes into crystalline form d if the water is removed, practically by azeotropic distillation, preferably at 35 to 37 DEG C, and stirring continues for at least 15 h at 30 to 45 DEG C, preferably 35 to 37 DEG C. Crystalline form d can also be obtained by stirring crystalline form a or ss in tert-butyl methyl ether containing 0.9 to 1.4 percent (v/v) of water at 33 to 38 DEG C while inoculating the same with crystalline form d. Crystalline form e can further be obtained by stirring crystalline form a or ss in tert-butyl methyl ether containing 0.9 to 1.4 percent (v/v) of water at 28 to 35 DEG C while inoculating the same with crystalline form e, or by stirring crystalline form a or ss in tert-butyl methyl ether containing 1.5 to 2.0 percent (v/v) of water at 35 to 38 DEG C.
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