Enantiomer (-) of tenatoprazole and the therapeutic use thereof
    3.
    发明授权
    Enantiomer (-) of tenatoprazole and the therapeutic use thereof 失效
    硝格拉唑的对映异构体( - )及其治疗用途

    公开(公告)号:US07652034B2

    公开(公告)日:2010-01-26

    申请号:US11344212

    申请日:2006-02-01

    IPC分类号: A61K31/48

    CPC分类号: C07D471/04

    摘要: The invention relates to enantiomer (−) of tentoprazole. The inventive enantiomer (−) of tenatoprazole, or (−)-5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridyl)methyl]sulfinyl]imidazol[4,5-b]pyridine exhibits improved pharmacokinetic properties which make it possible to use a once a day posology of a drug for relevant indications. The enantiomer (−) of tentoprazole can be used for treating digestive pathologies.

    摘要翻译: 本发明涉及吡喹啉的对映异构体( - )。 ( - ) - 5-甲氧基-2 - [[(4-甲氧基-3,5-二甲基-2-吡啶基)甲基]亚磺酰基]咪唑并[4,5-b]吡啶的本发明对映异构体( - ) 表现出改善的药代动力学性质,这使得可以使用药物的一天一次药物用于相关适应症。 托吡唑的对映异构体( - )可用于治疗消化性病变。

    Method for the enantioselective preparation of sulphoxide derivatives
    4.
    发明申请
    Method for the enantioselective preparation of sulphoxide derivatives 审中-公开
    亚砜衍生物对映选择性制备方法

    公开(公告)号:US20060281782A1

    公开(公告)日:2006-12-14

    申请号:US10551037

    申请日:2004-03-26

    CPC分类号: C07D471/04

    摘要: The invention relates to a method for the enantioselective preparation of substituted sulphoxide derivatives. The method comprises carrying out an enantioselective oxidation of a sulphide of general formula (I): A-CH2—S—B (I), where A=a variously-substituted pyridyl nucleus and B=a heterocyclic group with a benzimidazole or imidazopyrdyl nucleus, by means of an oxidising agent in the presence of a catalyst based on tungsten or vanadium and a chiral ligand, followed, where necessary, by salt formation with a base to give the sulphoxide: A-CH2—SO—B (Ia). The above is of application to the enantioselective preparation of compounds such as the enantiomers of tenatoprazole and other comparable sulphoxides.

    摘要翻译: 本发明涉及取代亚硫酰衍生物的对映选择性制备方法。 该方法包括进行通式(I)的硫化物的对映选择性氧化:A-CH2-SB(I),其中A =各种取代的吡啶基核,B =与苯并咪唑或咪唑并吡啶核的杂环基,通过 在基于钨或钒的催化剂和手性配体的存在下,氧化剂的手段,必要时通过与碱形成盐以产生亚砜:A-CH2-SO-B(Ia)。 以上是适用于化合物的对映体选择性制备,例如那格拉唑和其他可比较的亚砜的对映异构体。

    Method For Enantioselective Preparation Of Sulphoxide Derivatives
    5.
    发明申请
    Method For Enantioselective Preparation Of Sulphoxide Derivatives 失效
    亚砜衍生物的对映选择性制备方法

    公开(公告)号:US20070299261A1

    公开(公告)日:2007-12-27

    申请号:US11663647

    申请日:2005-10-05

    IPC分类号: C07D471/04

    摘要: The present invention concerns enantioselective preparation of sulphoxide derivatives or their salts. The method consist in performing an enantioselective oxidation of a sulphur of general formula (I) A-CH2—SB, wherein: A is a diversely substituted pyridinyl ring and B is a heterocyclic radical comprising an imidazo-pyridinyl ring, using an oxidizing agent in the presence of a titanium (IV)-based catalyst and a chiral ligand consisting of a cyclic beta or gamma-amino-alcohol, in an organic solvent, followed, if required, by salt formation with a base. The invention is useful for preparing sulphoxides useful in therapeutics.

    摘要翻译: 本发明涉及亚砜衍生物或其盐的对映选择性制备。 该方法包括对通式(I)A-CH 2 -SB的硫进行对映选择性氧化,其中:A是不同取代的吡啶基环,B是包含咪唑基 - 吡啶基环,使用氧化剂在有机溶剂中,在有机溶剂中,在有机溶剂中存在基于钛(IV)的催化剂和由环状β或γ-氨基醇组成的手性配体,然后如果 需要通过与碱形成盐。 本发明可用于制备用于治疗的亚砜。