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1.Process for the production of N-.beta.-hydroxyalkyl-tri-N-carboxyalkyl-1,4,7,10-tetraazacyclododecane and N-.beta.-hydroxyalkyl-tri-N-carboxyalkyl-1,4,8,11-tetraazacyclotetradeca ne derivatives and their metal complexes 失效
标题翻译: 制备N-β-羟基烷基 - 三-N-羧基烷基-1,4,7,10-四氮杂环十二烷和N-β-羟烷基 - 三-N-羧基烷基-1,4,8,11-四氮杂环十四烷衍生物的方法和 他们的金属配合物公开(公告)号:US5386028A
公开(公告)日:1995-01-31
申请号:US16452
申请日:1993-02-11
申请人: Ulf Tilstam , Helmut Borner , Klaus Nickisch , Heinz Gries , Johannes Platzek
发明人: Ulf Tilstam , Helmut Borner , Klaus Nickisch , Heinz Gries , Johannes Platzek
IPC分类号: A61K31/395 , A61K31/555 , A61K51/00 , C07D257/02 , C07D405/04 , C07F5/00 , C08F4/64 , A61K49/02
CPC分类号: C07D405/04 , C07D257/02
摘要: A process for the production of N-.beta.-hydroxyalkyl-tri-N-carboxyalkyl-1,4,7,10-tetraazacyclododecane and N-.beta.-hydroxyalkyl-tri-N-carboxyalkyl-1,4,8,11-tetraazacyclotetradecane derivatives and their metal complexes is described.
摘要翻译: 制备N-β-羟基烷基 - 三-N-羧基烷基-1,4,7,10-四氮杂环十二烷和N-β-羟烷基 - 三-N-羧基烷基-1,4,8,11-四氮杂环十四烷衍生物的方法 并描述了它们的金属络合物。
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2.Process for the production of fludarabine-phosphate lithium, sodium, potassium, calcium and magnesium salts and purification process for the production of fludarabine-phosphate and fludarabine-phosphate with a purity of at least 99.5% 有权
标题翻译: 用于生产氟达拉滨磷酸锂,钠,钾,钙和镁盐的方法和用于生产纯度至少为99.5%的氟达拉滨磷酸盐和氟达拉滨磷酸盐的纯化方法公开(公告)号:US07547776B1
公开(公告)日:2009-06-16
申请号:US09471040
申请日:1999-12-23
申请人: Ulf Tilstam , Thomas Schmitz , Klaus Nickisch
发明人: Ulf Tilstam , Thomas Schmitz , Klaus Nickisch
摘要: The present invention generally relates to a fludarabine-phosphate with a purity of at least 99.5%.
摘要翻译: 本发明一般涉及纯度至少为99.5%的氟达拉滨磷酸盐。
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3.Method for the production of imidazo-(1,2-C)(2,3)-benzodiazepines and intermediates in the production thereof 失效
标题翻译: 制备咪唑并(1,2-C)(2,3) - 苯并二氮杂的方法及其制备方法公开(公告)号:US06784292B2
公开(公告)日:2004-08-31
申请号:US10344156
申请日:2003-08-21
申请人: Eric Winter , Matthias Schneider , Ulf Tilstam
发明人: Eric Winter , Matthias Schneider , Ulf Tilstam
IPC分类号: C07D48704
CPC分类号: C07D487/04 , C07D263/32 , C07D317/60 , C07D413/06 , C07D491/14
摘要: The invention relates to a method for the preparation of compound of formula (1). The invention further relates to the previously unknown compounds of formulas (5 and 6) as intermediates in the production of benzodiazepines of formula (1).
摘要翻译: 本发明涉及制备式(1)化合物的方法。 本发明还涉及作为制备式(1)的苯并二氮杂类的中间体的式(5和6)的先前未知的化合物。
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4.Method for preparing 4-[17β-methoxy-17α-methoxymethyl-3-oxoestra-4,9-dien-11β-yl]benzaldehyde (E)-oxime (asoprisnil) 有权
标题翻译: 制备4- [17β-甲氧基-17α-甲氧基甲基-3-氧代雌-4,9-二烯-11β-基]苯甲醛(E) - 肟(asoprisnil)的方法,公开(公告)号:US08324412B2
公开(公告)日:2012-12-04
申请号:US12987850
申请日:2011-01-10
申请人: Detlef Grawe , Sabine Gliesing , Hagen Gerecke , Peter Hoesel , Uwe Mueller , Thomas Michel , Robert Eilers , Uwe Knabe , Bernd Erhart , Michael Mosebach , David Voigtlaender , Ulf Tilstam , Jürgen Jacke , Klaus Bahl , Ulf Bohlmann , Dieter Wehmeier , Michael Sander
发明人: Detlef Grawe , Sabine Gliesing , Hagen Gerecke , Peter Hoesel , Uwe Mueller , Thomas Michel , Robert Eilers , Uwe Knabe , Bernd Erhart , Michael Mosebach , David Voigtlaender , Ulf Tilstam , Jürgen Jacke , Klaus Bahl , Ulf Bohlmann , Dieter Wehmeier , Michael Sander
IPC分类号: C07J1/00
CPC分类号: C07J3/00 , Y10T428/2982
摘要: The present invention relates to a method for the reliable and reproducible preparation of 4-[17β-methoxy-17α-methoxymethyl-3-oxoestra-4,9-dien-11β-yl]benzaldehyde (E)-oxime (asoprisnil) on the pilot and manufacturing scale. Asoprisnil, which is prepared by this method, is distinguished by a very good physical stability and is therefore particularly suitable for the manufacture of solid pharmaceutical forms (tablets, coated tablets, etc.).
摘要翻译: 本发明涉及一种可靠和可重复制备4- [17-甲氧基-17α-甲氧基甲基-3-氧代雌-4,9-二烯-11-基]苯甲醛(E) - 肟(asoprisnil)的方法, 在试点和制造规模上。 通过该方法制备的麻醉药具有非常好的物理稳定性,因此特别适用于制备固体药物形式(片剂,包衣片剂等)。
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5.METHOD FOR PREPARING 4-[17BETA-METHOXY-17ALPHA-METHOXYMETHYL-3-OXOESTRA-4,9-DIEN-11-BETA-YL]BENZALDEHYDE (E)-OXIME (ASOPRISNIL) 有权
标题翻译: 制备4- [17-甲氧基-17α-甲氧基甲基-3-氧杂环丙烷-4,9-二烯-11-β-YL]苯甲醛(E)-OXIME(ASOPRISNIL)公开(公告)号:US20110257142A1
公开(公告)日:2011-10-20
申请号:US12987850
申请日:2011-01-10
申请人: Detlef Grawe , Sabine Gliesing , Hagen Gerecke , Peter Hoesel , Uwe Mueller , Thomas Michel , Robert Eilers , Uwe Knabe , Bernd Erhart , Michael Mosebach , David Voigtlaender , Ulf Tilstam , Jürgen Jacke , Klaus Bahl , Ulf Bohlmann , Dieter Wehmeier , Michael Sander
发明人: Detlef Grawe , Sabine Gliesing , Hagen Gerecke , Peter Hoesel , Uwe Mueller , Thomas Michel , Robert Eilers , Uwe Knabe , Bernd Erhart , Michael Mosebach , David Voigtlaender , Ulf Tilstam , Jürgen Jacke , Klaus Bahl , Ulf Bohlmann , Dieter Wehmeier , Michael Sander
CPC分类号: C07J3/00 , Y10T428/2982
摘要: The present invention relates to a method for the reliable and reproducible preparation of 4-[17β-methoxy-17α-methoxymethyl-3-oxoestra-4,9-dien-11β-yl]benzaldehyde (E)-oxime (asoprisnil) on the pilot and manufacturing scale. Asoprisnil, which is prepared by this method, is distinguished by a very good physical stability and is therefore particularly suitable for the manufacture of solid pharmaceutical forms (tablets, coated tablets, etc.).
摘要翻译: 本发明涉及一种可靠和可重复制备4- [17-甲氧基-17α-甲氧基甲基-3-氧代雌-4,9-二烯-11-基]苯甲醛(E) - 肟(asoprisnil)的方法, 在试点和制造规模上。 通过该方法制备的麻醉药具有非常好的物理稳定性,因此特别适用于制备固体药物形式(片剂,包衣片剂等)。
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6.Process for the production of fludarabine-phosphate lithium, sodium, potassium, calcium and magnesium salts and purification process for the production of fludarabine-phosphate and fludarabine-phosphate with a purity of at least 99.5% 有权
标题翻译: 用于生产氟达拉滨磷酸锂,钠,钾,钙和镁盐的方法和用于生产纯度至少为99.5%的氟达拉滨磷酸盐和氟达拉滨磷酸盐的纯化方法公开(公告)号:US6046322A
公开(公告)日:2000-04-04
申请号:US208587
申请日:1998-12-10
申请人: Ulf Tilstam , Thomas Schmitz , Klaus Nickisch
发明人: Ulf Tilstam , Thomas Schmitz , Klaus Nickisch
IPC分类号: C07H19/20 , C07H19/00 , C07H19/16 , C07H1/02 , C07H19/167
摘要: A reduced temperature crystallization process for the obtaining fludarabine phosphate at a purity of at least 99.5%.
摘要翻译: 用于获得纯度至少为99.5%的氟达拉滨磷酸盐的降温结晶方法。
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