S-Omeprazole Magnesium
    1.
    发明申请
    S-Omeprazole Magnesium 有权
    S-奥美拉唑镁

    公开(公告)号:US20100087652A1

    公开(公告)日:2010-04-08

    申请号:US12416537

    申请日:2009-04-01

    IPC分类号: C07D401/12

    CPC分类号: C07D401/12

    摘要: The present invention discloses a process for preparing a magnesium salt of S-omeprazole. The S-omeprazole salt preferably has a water content below about 4.8% by weight, a magnesium content of about 3.4-4.0% by weight, calculated on the weight of anhydrous, solvent free S-omeprazole magnesium, and has an optical purity of at least about 85% entantiomeric excess (“e.e.”). In addition, the present invention provides a magnesium salt of S-omeprazole which is substantially free of neutral omeprazole, meaning that the product contains less than about 3% by weight of a sum of neutral S-omeprazole and neutral omeprazole. Moreover, the S-omeprazole magnesium according to the invention preferably has assay of related substances and degradation products of less than about 0.1% by weight as determined by high performance liquid chromatography (HPLC).

    摘要翻译: 本发明公开了一种制备S-奥美拉唑镁盐的方法。 S-奥美拉唑盐的水含量优选低于约4.8重量%,镁含量为约3.4-4.0重量%,以无水,无溶剂的S-奥美拉唑镁的重量计,其光学纯度为 至少约85%的对映异构体过量(“ee”)。 此外,本发明提供了基本上不含中性奥美拉唑的S-奥美拉唑的镁盐,意味着该产品含有小于约3重量%的中性S-奥美拉唑和中性奥美拉唑的总和。 此外,根据本发明的S-奥美拉唑镁优选具有通过高效液相色谱(HPLC)测定的相关物质和降解产物的测定值小于约0.1重量%。

    Process for solvent removal from omeprazole salts
    2.
    发明授权
    Process for solvent removal from omeprazole salts 失效
    从奥美拉唑盐中去除溶剂的方法

    公开(公告)号:US08247567B2

    公开(公告)日:2012-08-21

    申请号:US12523025

    申请日:2008-01-09

    IPC分类号: C07D401/12

    CPC分类号: C07D401/12

    摘要: The present invention relates to a process for removing an organic solvent from a salt of omeprazole, in particular a magnesium salt of omeprazole, a composition comprising a salt of omeprazole, in particular a magnesium salt of omeprazole obtainable by such a process, and pharmaceutical compositions comprising said composition or a salt of omeprazole, in particular a magnesium salt of omeprazole, in particular where omeprazole is S-omeprazole.

    摘要翻译: 本发明涉及从奥美拉唑盐,特别是奥美拉唑镁盐中除去有机溶剂的方法,包含奥美拉唑盐,特别是可通过这种方法获得的奥美拉唑镁盐的组合物和药物组合物 包括所述组合物或奥美拉唑的盐,特别是奥美拉唑的镁盐,特别是奥美拉唑是S-奥美拉唑。

    S-omeprazole magnesium
    3.
    发明授权
    S-omeprazole magnesium 有权
    S-奥美拉唑镁

    公开(公告)号:US07875723B2

    公开(公告)日:2011-01-25

    申请号:US12416537

    申请日:2009-04-01

    IPC分类号: C07D401/12

    CPC分类号: C07D401/12

    摘要: The present invention discloses a process for preparing a magnesium salt of S-omeprazole. The S-omeprazole salt preferably has a water content below about 4.8% by weight, a magnesium content of about 3.4-4.0% by weight, calculated on the weight of anhydrous, solvent free S-omeprazole magnesium, and has an optical purity of at least about 85% entantiomeric excess (“e.e.”). In addition, the present invention provides a magnesium salt of S-omeprazole which is substantially free of neutral omeprazole, meaning that the product contains less than about 3% by weight of a sum of neutral S-omeprazole and neutral omeprazole. Moreover, the S-omeprazole magnesium according to the invention preferably has assay of related substances and degradation products of less than about 0.1% by weight as determined by high performance liquid chromatography (HPLC).

    摘要翻译: 本发明公开了一种制备S-奥美拉唑镁盐的方法。 S-奥美拉唑盐的水含量优选低于约4.8重量%,镁含量为约3.4-4.0重量%,以无水,无溶剂的S-奥美拉唑镁的重量计,其光学纯度为 至少约85%的对映异构体过量(“ee”)。 此外,本发明提供了基本上不含中性奥美拉唑的S-奥美拉唑的镁盐,意味着该产品含有小于约3重量%的中性S-奥美拉唑和中性奥美拉唑的总和。 此外,根据本发明的S-奥美拉唑镁优选具有通过高效液相色谱(HPLC)测定的相关物质和降解产物的测定值小于约0.1重量%。

    PROCESS FOR SOLVENT REMOVAL FROM OMEPRAZOLE SALTS
    4.
    发明申请
    PROCESS FOR SOLVENT REMOVAL FROM OMEPRAZOLE SALTS 失效
    从OMEPRAZOLE SALTS去除溶剂的方法

    公开(公告)号:US20100076025A1

    公开(公告)日:2010-03-25

    申请号:US12523025

    申请日:2008-01-09

    CPC分类号: C07D401/12

    摘要: The present invention relates to a process for removing an organic solvent from a salt of omeprazole, in particular a magnesium salt of omeprazole, a composition comprising a salt of omeprazole, in particular a magnesium salt of omeprazole obtainable by such a process, and pharmaceutical compositions comprising said composition or a salt of omeprazole, in particular a magnesium salt of omeprazole, in particular where omeprazole is S-omeprazole.

    摘要翻译: 本发明涉及从奥美拉唑盐,特别是奥美拉唑镁盐中除去有机溶剂的方法,包含奥美拉唑盐,特别是可通过这种方法获得的奥美拉唑镁盐的组合物和药物组合物 包括所述组合物或奥美拉唑的盐,特别是奥美拉唑的镁盐,特别是奥美拉唑是S-奥美拉唑。

    S-omeprazole magnesium
    5.
    发明授权
    S-omeprazole magnesium 失效
    S-奥美拉唑镁

    公开(公告)号:US07553857B2

    公开(公告)日:2009-06-30

    申请号:US11318236

    申请日:2005-12-23

    IPC分类号: A61K31/4439 C07D401/12

    CPC分类号: C07D401/12

    摘要: The present invention discloses a process for preparing a magnesium salt of S-omeprazole. The S-omeprazole salt preferably has a water content below about 4.8% by weight, a magnesium content of about 3.4-4.0% by weight, calculated on the weight of anhydrous, solvent free S-omeprazole magnesium, and has an optical purity of at least about 85% entantiomeric excess (“e.e.”). In addition, the present invention provides a magnesium salt of S-omeprazole which is substantially free of neutral omeprazole, meaning that the product contains less than about 3% by weight of a-sum of neutral S-omeprazole and neutral omeprazole. Moreover, the S-omeprazole magnesium according to the invention preferably has assay of related substances and degradation products of less than about 0.1 % by weight as determined by high performance liquid chromatography (HPLC).

    摘要翻译: 本发明公开了一种制备S-奥美拉唑镁盐的方法。 S-奥美拉唑盐的水含量优选低于约4.8重量%,镁含量为约3.4-4.0重量%,以无水,无溶剂的S-奥美拉唑镁的重量计,其光学纯度为 至少约85%的对映异构体过量(“ee”)。 此外,本发明提供了基本上不含中性奥美拉唑的S-奥美拉唑镁盐,意味着该产品含有小于约3重量%的中和S-奥美拉唑和中性奥美拉唑的总和。 此外,根据本发明的S-奥美拉唑镁优选具有通过高效液相色谱(HPLC)测定的相关物质和降解产物的测定值小于约0.1重量%。

    Process for the preparation of enantiomerically enriched proton pump inhibitors
    6.
    发明授权
    Process for the preparation of enantiomerically enriched proton pump inhibitors 有权
    用于制备对映体富集的质子泵抑制剂的方法

    公开(公告)号:US08889873B2

    公开(公告)日:2014-11-18

    申请号:US13124082

    申请日:2009-10-13

    IPC分类号: C07D401/12

    CPC分类号: C07D401/12

    摘要: The invention discloses a process for the preparation of compounds having structures typical for proton pump inhibitors in enantiomerically enriched form by using particular metal catalysts in an enantioselective oxidation step. Also disclosed are useful further processes and pure intermediate and subsequently final products.

    摘要翻译: 本发明公开了一种通过在对映选择性氧化步骤中使用特定的金属催化剂来制备具有对映体富集形式的质子泵抑制剂典型结构的化合物的方法。 还公开了有用的进一步方法和纯中间体和随后的最终产物。

    PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY ENRICHED PROTON PUMP INHIBITORS
    7.
    发明申请
    PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY ENRICHED PROTON PUMP INHIBITORS 有权
    制备高效液相色谱泵抑制剂的方法

    公开(公告)号:US20120046319A1

    公开(公告)日:2012-02-23

    申请号:US13124082

    申请日:2009-10-13

    CPC分类号: C07D401/12

    摘要: The invention discloses a process for the preparation of compounds having structures typical for proton pump inhibitors in enantiomerically enriched form by using particular metal catalysts in an enantioselective oxidation step. Also disclosed are useful further processes and pure intermediate and subsequently final products.

    摘要翻译: 本发明公开了一种通过在对映选择性氧化步骤中使用特定的金属催化剂来制备具有对映体富集形式的质子泵抑制剂典型结构的化合物的方法。 还公开了有用的进一步方法和纯中间体和随后的最终产物。

    Process for the preparation of esomeprazole magnesium in a stable form
    8.
    发明授权
    Process for the preparation of esomeprazole magnesium in a stable form 失效
    以稳定形式制备艾美拉唑镁的方法

    公开(公告)号:US08362259B2

    公开(公告)日:2013-01-29

    申请号:US12506662

    申请日:2009-07-21

    IPC分类号: C07D401/12

    CPC分类号: C07D401/12

    摘要: There is provided a process for preparing purified esomeprazole magnesium, comprising the steps of: providing esomeprazole magnesium; contacting said esomeprazole magnesium with a non-solvent comprising an aqueous component up to a maximum content defined by water saturation in the non-solvent; and recovering purified esomeprazole magnesium formed from the contacting step. The process is particularly suitable to obtain esomeprazole magnesium dihydrate, especially form A. The esomeprazole magnesium obtained is remarkably pure, stable and is resistant to form interchangeability.

    摘要翻译: 提供了制备纯化的艾美拉唑镁的方法,包括以下步骤:提供艾美拉唑镁; 使所述艾美拉唑镁与包含水性组分的非溶剂接触,直到在非溶剂中由水饱和度限定的最大含量; 并回收由接触步骤形成的纯化的埃索美拉唑镁。 该方法特别适用于获得艾美拉唑镁二水合物,特别是A型。所得到的艾美拉唑镁非常纯净,稳定,具有互换性。

    PROCESS FOR THE PREPARATION OF ESOMEPRAZOLE MAGNESIUM IN A STABLE FORM
    10.
    发明申请
    PROCESS FOR THE PREPARATION OF ESOMEPRAZOLE MAGNESIUM IN A STABLE FORM 失效
    在稳定形式中制备异喹诺酮的方法

    公开(公告)号:US20100016370A1

    公开(公告)日:2010-01-21

    申请号:US12506662

    申请日:2009-07-21

    CPC分类号: C07D401/12

    摘要: There is provided a process for preparing purified esomeprazole magnesium, comprising the steps of: providing esomeprazole magnesium; contacting said esomeprazole magnesium with a non-solvent comprising an aqueous component up to a maximum content defined by water saturation in the non-solvent; and recovering purified esomeprazole magnesium formed from the contacting step. The process is particularly suitable to obtain esomeprazole magnesium dihydrate, especially form A. The esomeprazole magnesium obtained is remarkably pure, stable and is resistant to form interchangeability.

    摘要翻译: 提供了制备纯化的艾美拉唑镁的方法,包括以下步骤:提供艾美拉唑镁; 使所述艾美拉唑镁与包含水性组分的非溶剂接触,直到在非溶剂中由水饱和度限定的最大含量; 并回收由接触步骤形成的纯化的埃索美拉唑镁。 该方法特别适用于获得艾美拉唑镁二水合物,特别是A型。所得到的艾美拉唑镁非常纯净,稳定,具有互换性。