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1. 发明申请

WO2009080227A3 PYRAZOLE-CARBOXAMIDE DERIVATIVES AS P2Y12 ANTAGONISTS 审中-公开
公开(公告)号：WO2009080227A3
公开(公告)日：2009-07-02
申请号：PCT/EP2008/010573
申请日：2008-12-12
申请人： SANOFI-AVENTIS , NAZARÉ, Marc , ZECH, Gernot , GOERLITZER, Jochen , JUST, Melitta , WEISS, Tilo , HESSLER, Gerhard , CZECHTIZKY, Werngard , RUF, Sven
发明人： NAZARÉ, Marc , ZECH, Gernot , GOERLITZER, Jochen , JUST, Melitta , WEISS, Tilo , HESSLER, Gerhard , CZECHTIZKY, Werngard , RUF, Sven
IPC分类号： C07D403/12 , A61K31/496 , A61P7/02
摘要： The present invention relates to compounds of the Formula (I), wherein R1; R2; Z; A; B; D; Q; J; V; G and M have the meanings indicated in the claims. The compounds of the formula I are valuable pharmacologically active compounds. They exhibit a strong anti-aggregating effect on platelets and thus an anti-thrombotic effect and are suitable e.g. for the therapy and prophylaxis of cardio-vascular disorders like thromboembolic diseases or restenoses. They are reversible antagonists of the platelet ADP receptor P2Y12, and can in general be applied in conditions in which an undesired activation of the platelet ADP receptor P2Y12 is present or for the cure or prevention of which an inhibition of the platelet ADP receptor P2Y12 is intended. The invention furthermore relates to processes for the preparation of compounds of the Formula (I), their use, in particular as active ingredients in pharmaceuticals, and pharmaceutical preparations comprising them.

2. 发明申请

WO2009000411A1 A TRANSITION METAL CATALYZED SYNTHESIS OF 2H-INDAZOLES 审中-公开
标题翻译： 2H-INDAZOLES的过渡金属催化合成
公开(公告)号：WO2009000411A1
公开(公告)日：2008-12-31
申请号：PCT/EP2008/004637
申请日：2008-06-11
申请人： SANOFI-AVENTIS , HALLAND, Nis , NAZARÉ, Marc , LINDENSCHMIDT, Andreas , ALONSO, Jorge , R'KYEK, Omar , URMANN, Matthias
发明人： HALLAND, Nis , NAZARÉ, Marc , LINDENSCHMIDT, Andreas , ALONSO, Jorge , R'KYEK, Omar , URMANN, Matthias
IPC分类号： C07D231/56
CPC分类号： C07D231/56
摘要： The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), wherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4; Q and J have the meanings indicated in the claims. The present invention provides a direct transition metal catalyzed process to a wide variety of multifunctional 2H-indazoles or 2H-azaindazoles of the formula (I) from 2-halo-phenylacetylenes or (2-sulfonato)phenylacetylenes and monosubstituted hydrazines, useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides.
摘要翻译：本发明涉及一种用于区域选择性合成式（I）化合物的方法，其中R 0; R1; R2; R3; R4; R5; A1; A2; A3; A4; Q和J具有权利要求中所示的含义。本发明提供了一种直接过渡金属催化的方法，用于从2-卤代 - 苯基乙炔或（2-磺酸基）苯基乙炔和单取代的肼的多种多功能2H-吲唑或式（I）的2H-氮杂吲唑，其可用于生产药物，诊断剂，液晶，聚合物，除草剂，杀真菌剂，杀线虫剂，杀寄生虫剂，杀虫剂，杀螨剂和节肢动物杀虫剂。

3. 发明申请

WO2005085239A2 PYRROLE-DERIVATIVES AS FACTOR Xa INHIBITORS 审中-公开
标题翻译：吡咯衍生物作为因子Xa抑制剂
公开(公告)号：WO2005085239A2
公开(公告)日：2005-09-15
申请号：PCT/EP2005/001423
申请日：2005-02-12
申请人： AVENTIS PHARMA DEUTSCHLAND GMBH , BAUER, Armin , WAGNER, Michael , NAZARÉ, Marc , WEHNER, Volkmar , URMANN, Matthias , MATTER, Hans
发明人： BAUER, Armin , WAGNER, Michael , NAZARÉ, Marc , WEHNER, Volkmar , URMANN, Matthias , MATTER, Hans
IPC分类号： C07D413/14
CPC分类号： C07D401/12 , C07D401/14 , C07D413/14
摘要： The present invention relates to compounds of the formulae (I) and (Ia), wherein R 0 ; R 1 ; R3; R4; R22, Q; V, G and M have the meanings indicated in the claims. The compounds of the formulae (I) and (Ia) are valuable pharmacologically active compounds. They exhibit a strong antithrombotic effect and are suitable for the therapy and prophylaxis of cardiovascular disorders like thromboembolic diseases or restenoses. They are reversible inhibitors of the blood clotting enzymes factor Xa (FXa) and/or factor VIIa (FVIIa), and can in general be applied in conditions in which an undesired activity of factor Xa and/or factor VIIa is present or for the cure or prevention of which an inhibition of factor Xa and/or factor VIIa is intended. The invention furthermore relates to processes for the preparation of compounds of the formulae (I) and (Ia), their use, in particular as active ingredients in pharmaceuticals, and pharmaceutical preparations comprising them.
摘要翻译：本发明涉及式（I）和（Ia）的化合物，其中R为0; [R ^{1 ; R3; R4; R22，Q; V，G和M具有权利要求中所表示的含义。式（I）和（Ia）的化合物是有价值的药理活性化合物。它们表现出强烈的抗血栓作用，适用于心血管疾病如血栓栓塞性疾病或再狭窄的治疗和预防。它们是凝血酶因子Xa（FXa）和/或因子VIIa（FVIIa）的可逆抑制剂，并且通常可以用于其中存在不想要的因子Xa和/或因子VIIa活性的条件或用于治疗或预防因子Xa和/或因子VIIa的抑制。本发明还涉及制备式（I）和（Ia）化合物的方法，其用途，特别是作为药物中的活性成分以及包含它们的药物制剂。}

4. 发明申请

WO2008009348A1 A REGIOSELECTIVE PALLADIUM CATALYZED SYNTHESIS OF BENZIMIDAZOLES AND AZABENZIMIDAZOLES 审中-公开
标题翻译：苯并咪唑和AZABENZIMIDAZOLES的选择性催化合成
公开(公告)号：WO2008009348A1
公开(公告)日：2008-01-24
申请号：PCT/EP2007/005816
申请日：2007-06-30
申请人： SANOFI-AVENTIS , ALONSO, Jorge , LINDENSCHMIDT, Andreas , NAZARÉ, Marc , HALLAND, Nis , RKYEK, Omar , URMANN, Matthias
发明人： ALONSO, Jorge , LINDENSCHMIDT, Andreas , NAZARÉ, Marc , HALLAND, Nis , RKYEK, Omar , URMANN, Matthias
IPC分类号： C07D235/10 , C07D235/12 , C07D235/08 , C07D235/02 , C07D487/04
CPC分类号： C07D235/10 , C07D235/08 , C07D235/16 , C07D401/04 , C07D471/04
摘要： The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), wherein RO; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct palladium catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N -substituted benzimidazoles or azabenzimidazoles of formula (I) starting from 2-halo-nitroarenes and Λ/-substituted amides useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricitdes and arthropodicides.
摘要翻译：本发明涉及一种用于区域选择性合成式（I）化合物的方法，其中RO; R1; R2; R3; R4; R5; A1; A2; A3; A4，Q和J具有权利要求中所示的含义。本发明提供了直接钯催化的区域选择性方法，其可从用于制备药物的2-卤代 - 硝基芳烃和β-取代的酰胺开始，从多种不对称，多官能的式（I）的N-取代的苯并咪唑或氮杂苯并咪唑开始，诊断剂，液晶，聚合物，除草剂，杀真菌剂，杀线虫剂，杀寄生虫剂，杀虫剂，螨类和节肢动物杀虫剂。

5. 发明申请

WO2005095440A1 BETA-AMINOACID-DERIVATIVES AS FACTOR Xa INHIBITORS 审中-公开
标题翻译： β-氨基酸衍生物作为因子Xa抑制剂
公开(公告)号：WO2005095440A1
公开(公告)日：2005-10-13
申请号：PCT/EP2005/001736
申请日：2005-02-19
申请人： AVENTIS PHARMA DEUTSCHLAND GMBH , URMANN, Matthias , NAZARÉ, Marc , WEHNER, Volkmar , MATTER, Hans , BAUER, Armin , WAGNER, Michael
发明人： URMANN, Matthias , NAZARÉ, Marc , WEHNER, Volkmar , MATTER, Hans , BAUER, Armin , WAGNER, Michael
IPC分类号： C07K5/02
CPC分类号： C07K5/0202 , C07D265/32 , C07D265/33 , C07D291/06 , C07D295/112 , C07D409/12 , C07D409/14 , C07D413/12 , C07D419/12
摘要： The present invention relates to compounds of the Formula (I), in which R ° ; R 1 ; R 2 ; R 3 ; R 4 ; R 5 ; R 6 ; Q; V; G and M have the meanings indicated in the claims. The compounds of the formula I are valuable pharmacologically active compounds. They exhibit a strong antithrombotic effect and are suitable, for example, for the therapy and prophylaxis of cardiovascular disorders like thromboembolic diseases or restenoses. They are reversible inhibitors of the blood clotting enzymes factor Xa (FXa) and/or factor VIIa (FVIIa), and can in general be applied in conditions in which an undesired activity of factor Xa and/or factor VIIa is present or for the cure or prevention of which an inhibition of factor Xa and/or factor VIIa is intended. The invention furthermore relates to processes for the preparation of compounds of the formula I, their use, in particular as active ingredients in pharmaceuticals, and pharmaceutical preparations comprising them.
摘要翻译：本发明涉及式（I）的化合物，其中R 1， [R <1>; [R <2>; [R <3>; [R <4>; [R <5>; [R <6>; Q; V; G和M具有权利要求中所示的含义。式I的化合物是有价值的药理活性化合物。它们具有强烈的抗血栓形成作用，并且适用于例如治疗和预防心血管疾病如血栓栓塞性疾病或再狭窄。它们是血液凝固酶因子Xa（FXa）和/或因子VIIa（FVIIa）的可逆抑制剂，并且通常可以在其中存在因子Xa和/或因子VIIa的不期望活性或用于治愈或预防因子Xa和/或因子VIIa的抑制。本发明还涉及制备式I化合物的方法，其用途，特别是作为药物中的活性成分，以及包含它们的药物制剂。

6. 发明申请

WO2013041119A1 N-[4-(1H-PYRAZOLO[3,4-B]PYRAZIN-6-YL)-PHENYL]-SULFONAMIDES AND THEIR USE AS PHARMACEUTICALS 审中-公开
标题翻译： N- [4-（1H-吡唑并[3,4-B]吡嗪-6-基） - 苯基] - 磺酰胺及其作为药物的用途
公开(公告)号：WO2013041119A1
公开(公告)日：2013-03-28
申请号：PCT/EP2011/066220
申请日：2011-09-19
申请人： SANOFI , NAZARÉ, Marc , HALLAND, Nis , SCHMIDT, Friedemann , WEISS, Tilo , DIETZ, Uwe , HOFMEISTER, Armin
发明人： NAZARÉ, Marc , HALLAND, Nis , SCHMIDT, Friedemann , WEISS, Tilo , DIETZ, Uwe , HOFMEISTER, Armin
IPC分类号： C07D487/04 , A61K31/4985 , A61P19/02
CPC分类号： C07D487/04
摘要： The present invention relates to N-[4-(1H-pyrazolo[3,4-b]pyrazin-6-yl)-phenyl]- sulfonamides of the formula I, wherein Ar, R1, R2 and n have the meanings indicated in the claims. The compounds of the formula I are valuable pharmacologically active compounds which modulate protein kinase activity, specifically the activity of serum and glucocorticoid regulated kinase (SGK), in particular of serum and glucocorticoid regulated kinase isoform 1 (SGK-1, SGK1), and are suitable for the treatment of diseases in which SGK activity is inappropriate, for example degenerative joint disorders or inflammatory processes such as osteoarthritis or rheumatism. The invention furthermore relates to processes for the preparation of the compounds of the formula I, their use as pharmaceuticals, and pharmaceutical compositions comprising them.
摘要翻译：本发明涉及式I的N- [4-（1H-吡唑并[3,4-b]吡嗪-6-基） - 苯基]磺酰胺，其中Ar，R 1，R 2和n具有如索赔。式I的化合物是调节蛋白激酶活性，特别是血清和糖皮质激素调节激酶（SGK）的活性，特别是血清和糖皮质激素调节激酶同工型1（SGK-1，SGK1）的活性的有价值的药理学活性化合物，并且是适用于治疗SGK活动不适当的疾病，例如退行性关节疾病或炎性过程如骨关节炎或风湿病。本发明还涉及式I化合物的制备方法，它们作为药物的用途，以及包含它们的药物组合物。

7. 发明申请

WO2009080226A2 HETEROCYCLIC PYRAZOLE-CARBOXAMIDES AS P2Y12 ANTAGONISTS 审中-公开
标题翻译：作为P2Y12拮抗剂的杂环吡唑类羧酰胺
公开(公告)号：WO2009080226A2
公开(公告)日：2009-07-02
申请号：PCT/EP2008/010572
申请日：2008-12-12
申请人： SANOFIS-AVENTIS , NAZARÉ, Marc , ZECH, Gernot , JUST, Melitta , WEISS, Tilo , HESSLER, Gerhard , KOHLMANN, Markus
发明人： NAZARÉ, Marc , ZECH, Gernot , JUST, Melitta , WEISS, Tilo , HESSLER, Gerhard , KOHLMANN, Markus
IPC分类号： C07D403/14 , A61K31/496 , A61P7/02
CPC分类号： C07D403/14
摘要： The present invention relates to compounds of the formula I, wherein R1; R2; Z; A; B; D; Q; J; V; G and M have the meanings indicated in the claims. The compounds of the formula I are valuable pharmacologically active compounds. They exhibit a strong anti-aggregating effect on platelets and thus an anti-thrombotic effect and are suitable e.g. for the therapy and prophylaxis of cardio-vascular disorders like thromboembolic diseases or restenoses. They are reversible antagonists of the platelet ADP receptor P2Y12, and can in general be applied in conditions in which an undesired activation of the platelet ADP receptor P2Y12 is present or for the cure or prevention of which an inhibition of the platelet ADP receptor P2Y12 is intended. The invention furthermore relates to processes for the preparation of compounds of the formula I, their use, in particular as active ingredients in pharmaceuticals, and pharmaceutical preparations comprising them.
摘要翻译：本发明涉及式I化合物，其中R1; R2; Z者除外; 一个; B; D组; Q; 焦耳; V; G和M具有权利要求中所示的含义。式I的化合物是有价值的药理活性化合物。它们对血小板表现出强烈的抗凝集作用，因此表现出抗血栓形成的作用，用于治疗和预防心血管疾病如血栓栓塞性疾病或再狭窄。它们是血小板ADP受体P2Y12的可逆拮抗剂，并且通常可用于其中存在血小板ADP受体P2Y12的不期望的活化或用于治疗或预防血小板ADP受体P2Y12的抑制的条件。本发明还涉及制备式I化合物的方法，其用途，特别是作为药物中的活性成分，以及包含它们的药物制剂。

8. 发明申请

WO2009000413A1 A REGIOSELECTIVE COPPER CATALYZED SYNTHESIS OF BENZIMIDAZOLES AND AZABENZIMIDAZOLES 审中-公开
标题翻译：苯并咪唑和氨苄青霉素的选择性铜催化合成
公开(公告)号：WO2009000413A1
公开(公告)日：2008-12-31
申请号：PCT/EP2008/004639
申请日：2008-06-11
申请人： SANOFI-AVENTIS , ALONSO, Jorge , LINDENSCHMIDT, Andreas , NAZARÉ, Marc , URMANN, Matthias , HALLAND, Nis , R'KYEK, Omar
发明人： ALONSO, Jorge , LINDENSCHMIDT, Andreas , NAZARÉ, Marc , URMANN, Matthias , HALLAND, Nis , R'KYEK, Omar
IPC分类号： C07D235/08 , C07D235/16 , C07D235/18 , C07D401/04 , C07D471/04
CPC分类号： C07D235/08 , C07D235/16 , C07D235/18 , C07D401/04 , C07D471/04
摘要： The present invention relates to a process for the regioselective synthesis of compounds of the formula (I), wherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4; Q and J have the meanings indicated in the claims. The present invention provides a direct copper catalyzed regioselective process to a wide variety of unsymmetrical, multifunctional N /-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N /-substituted amides. The process is useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides.
摘要翻译：本发明涉及一种用于区域选择性合成式（I）化合物的方法，其中R 0; R1; R2; R3; R4; R5; A1; A2; A3; A4; Q和J具有权利要求中所示的含义。本发明为从2-卤代 - 硝基芳烃和N-取代的酰胺开始的多种不对称的，多官能的N-取代的苯并咪唑或式I的氮杂苯并咪唑提供直接铜催化的区域选择性方法。该方法可用于生产药物，诊断剂，液晶，聚合物，除草剂，杀真菌剂，杀线虫剂，杀寄生虫剂，杀虫剂，杀螨剂和节肢动物杀虫剂。

9. 发明申请

WO2006122661A1 HETEROARYL-CARBOXYLIC ACID (SULFAMOYL ALKYL) AMIDE - DERIVATIVES AS FACTOR XA INHIBITORS 审中-公开
标题翻译：异硫氰酸（磺酰氨基）酰胺 - 衍生物作为因子XA抑制剂
公开(公告)号：WO2006122661A1
公开(公告)日：2006-11-23
申请号：PCT/EP2006/004255
申请日：2006-05-06
申请人： SANOFI-AVENTIS DEUTSCHLAND GMBH , WAGNER, Michael , URMANN, Matthias , WEHNER, Volkmar , LORENZ, Martin , BAUER, Armin , NAZARÉ, Marc , MATTER, Hans
发明人： WAGNER, Michael , URMANN, Matthias , WEHNER, Volkmar , LORENZ, Martin , BAUER, Armin , NAZARÉ, Marc , MATTER, Hans
IPC分类号： C07D409/12 , A61K31/4535 , A61P7/02 , C07D409/14 , C07D333/38 , C07D405/12 , C07D211/58 , C07D401/12 , C07D413/14 , C07D417/14 , C07D419/14
CPC分类号： C07D211/58 , C07D333/38 , C07D401/12 , C07D405/12 , C07D409/12 , C07D409/14 , C07D413/14 , C07D417/14 , C07D419/14
摘要： The present invention relates to compounds of the Formula (I), in which R1; R2; R3; V; G1 and G2 have the meanings indicated in the claims. The compounds of the formula (I) are valuable pharmacologically active compounds. They exhibit a strong antithrombotic effect and are suitable, for example, for the therapy and prophylaxis of cardiovascular disorders like thromboembolic diseases or restenoses. They are reversible inhibitors of the blood clotting enzymes factor Xa, and can in general be applied in conditions in which an undesired activity of factor Xa is present or for the cure or prevention of which an inhibition of factor Xa is intended. The invention furthermore relates to processes for the preparation of compounds of the formula (I), their use, in particular as active ingredients in pharmaceuticals, and pharmaceutical preparations comprising them.
摘要翻译：本发明涉及式（I）的化合物，其中R 1; R2; R3; V; G1和G2具有权利要求中所示的含义。式（I）的化合物是有价值的药理活性化合物。它们具有强烈的抗血栓形成作用，并且适用于例如治疗和预防心血管疾病如血栓栓塞性疾病或再狭窄。它们是血液凝固酶因子Xa的可逆抑制剂，并且通常可以在其中存在不需要的因子Xa的活性或用于治疗或预防因子Xa的抑制的条件下使用。本发明还涉及式（I）化合物的制备方法，其用途，特别是药物中的活性成分，以及包含它们的药物制剂。

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