发明名称 CRYSTALLINE [R-(R*, R*)]-2-(4-FLUOROPHENYL)-BETA, DELTA-DIHYDROXY-5-(1-METHYLETHYL)-3-PHENYL-4-[(PHENYLAMINO)CARBONYL]-1H-PYRROLE-1-HEPTANOIC ACID HEMI CALCIUM SALT (ATORVASTATIN)
摘要 1. A crystalline Form I atorvastatin or a hydrate thereof having an X-ray powder diffraction containing as a parent peak the following 2&theta; value measured using CuK&alpha; radiation: 21.6. 2. A crystalline Form 1 atorvastatin or a hydrate thereof according to Claim 1 further containing the following 2&theta; values measured using CuK&alpha; radiation: 17.1, 19.5 and 23.7. 3. A crystalline Form I atorvastatin or a hydrate thereof according to Claim 2 further containing the following 2&theta; values measured using CuK&alpha; radiation: 9.2, 9.5, 10.3, 11.9, 22.0, 22.7 and 23.3. 4. A crystalline Form I atorvastatin or a hydrate thereof having an X-ray powder diffraction containing the following 2&theta; values measured using CuK&alpha; radiation 9.2, 9.5, 10.3, 10.6, 11.9, 12.2, 17.1, 19.5, 21.6, 22.0, 22.7, 23.3, 23.7, 24.4, 28.9 and 29.2. 5. A crystalline Form I atorvastatin or a hydrate thereof having an X-ray powder diffraction containing at least one of the following 2&theta; values measured using CuK&alpha; radiation: 11.9 or 22.0. 6. A crystalline Form I atorvastatin or a hydrate thereof characterized by solid-state C<13> nuclear magnetic resonance having the following chemical shifts expressed in parts per million: 21.3, 25.2, 26.4, 40.2, 41.9, 47.4, 64.9, 68.1, 70.5, 73.1, 113.8, 118.2, 120.9, 123.5, 127.6, 129.5, 131.1, 134.9, 137.0, 159.3, 166.7 (broad), 178.4 and 182.8. 7. The crystalline Form I atorvastatin according to any one of the preceding Claims containing 1 to 8 moles of water. 8. The crystalline Form I atorvastatin according to any one of the preceding Claims containing 3 moles of water. 9. Crystalline Form II atorvastatin or a hydrate thereof having an X-ray powder diffraction containing as a parent peak the following 2&theta; value measured using CuK&alpha; radiation: 8.5. 10. Crystalline Form II atorvastatin or a hydrate thereof according to Claim 9 further containing the following 2&theta; values measured using CuK&alpha; radiation: 9.0 and 20.5. 11. Crystalline Form II atorvastatin or a hydrate thereof according to Claim 10 further containing the following 2&theta; values measured using CuK&alpha; radiation: 5.6, 17.1 - 17.4 (broad), 19.5 and 22.7 - 23.2 (broad). 12. Crystalline Form II atorvastatin or a hydrate thereof having an X-ray powder diffraction containing the following 2&theta; values measured using CuK&alpha; radiations 5.6, 7.4, 8.5, 9.0, 12.4 (broad), 15.8 (broad), 17.1 - 17.4 (broad), 19.5, 20.5, 22.7-23.2 (broad), 25.7 (broad) and 29.5. 13. Crystalline Form IX atcorvastabin or a hydrate thereof containing the following 2&theta; values measured using CuK&alpha; radiation: 9.0 and 20.5. 14. Crystalline Form II atorvastatin or a hydrate thereof characterized by solid-state C<13> nuclear magnetic resonance having the following chemical shifts expressed in parts per million: 22.8 (broad), 27.5, 40.2, 41.7, 42.3, 43.4, 67.3, 68.0, 69.0, 70.6, 114.7, 115.7, 117.1, 119.0, 120.3, 121.4, 122.9, 129.0, 133.3, 134.8, 140.5, 161 (broad), 163 (broad) and 181 (broad). 15. Crystalline Form IV atorvastatin or a hydrate thereof having an X-ray powder diffraction containing as a parent peak the following 2&theta; value measured using CuK&alpha; radiation: 8.0. 16. Crystalline Form IV atorvastatin or a hydrate thereof according to Claim l5 further containing the following 2&theta; value measured using CuK&alpha; radiation: 9.7. 17. Crystalline Form IV atorvastatin or a hydrate thereof according to Claim 16 further containing the following 2&theta; value measured using CuK&alpha; radiation; 19.6. 18. Crystalline Form IV atorvastatin or a hydrate thereof having an X-ray powder diffraction containing the following 2&theta; values measured using CuK&alpha; radiation: 4.9, 5.4, 5.9, 8.0, 9.7, 10.4, 12.4, 17.7, 18.4, 19.2, 19.6, 21.7, 23.0, 23.7 and 24.1. 19. Crystalline Form IV atorvastatin or a hydrate thereof having an X-ray powder diffraction containing at least one of the following 2&theta; value measured using CuK&alpha; radiation: 8.0 or 9.7. 20. Crystalline Forrn IV atorvastatin or a hydrate thereof characterized by solid-state <13>C nuclear magnetic resonance having the following chemical shifts expressed in parts per million: 17.9, 19.4, 20.3, 25.9, 40.0, 42.1, 43-4, 46.1, 63.5, 66.3, 67.9, 71.5, 115.7, 119.8, 122.7, 127.1, 129.2, 134.7, 138.1 (broad), 159.0 (broad), 166.1 (broad), 179.3, 181.4, 184.9 and 1S6.4. 21. A pharmaceutical composition comprising crystalline Form I, Form II or Form IV atorvastatin or a hydrate thereof according to any one of the preceding Claims in admixture with at least one pharmaceutically acceptable excipient, diluent or carrier. 22. A pharmaceutical composition according to Claim 21 in the form of tablets, pills, dispersible granules, cachete, capsules, powders, lozenges, suppositories or retentxon enemas.
申请公布号 EA000474(B1) 申请公布日期 1999.08.26
申请号 EA19980000130 申请日期 1996.07.08
申请人 WARNER-LAMBERT COMPANY 发明人 BRIGGS, CHRISTOPHER, A.;JENNINGS, REX, ALLEN;WADE, ROBERT, A.;HARASAWA, KIKUKO;ICHIKAWA, SHIGERU;MINOHARA, KAZUO;NAKAGAWA, SHINSUKE
分类号 C07D207/34;A61K31/40;A61P3/06;A61P3/14;A61P43/00;C07D 主分类号 C07D207/34
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