Pyramid | 358350-41-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡喃
• 英文名称: Pyramid
• 英文别名: 2H-pyran-2-carboxamide
• CAS: 358350-41-1
• 化学式: C₆H₇NO₂
• 分子量: 125.13
• InChiKey: MMTVHLPXGYWNOJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  9
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  52.3
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• [EN] HETEROARYL SUBSTITUTED HETEROCYCLYL SULFONES<br/>[FR] SULFONES À HÉTÉROCYCLYLES À SUBSTITUTION HÉTÉROARYLE
  申请人：GRUENENTHAL GMBH

  公开号：WO2015158427A1

  公开（公告）日：2015-10-22

  The invention relates to aryl substituted heterocyclyl sulfones as voltage gated calcium channel blockers, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.

  这项发明涉及芳基取代的杂环磺酮作为电压门控钙通道阻滞剂，以及含有这些化合物的药物组合物，还涉及这些化合物用于治疗和/或预防疼痛以及其他疾病和/或紊乱。
• [EN] BIARYL COMPOUNDS USEFUL FOR THE TREATMENT OF HUMAN DISEASES IN ONCOLOGY, NEUROLOGY AND IMMUNOLOGY<br/>[FR] COMPOSÉS BIARYLIQUES UTILES POUR LE TRAITEMENT DE MALADIES HUMAINES EN ONCOLOGIE, NEUROLOGIE ET IMMUNOLOGIE
  申请人：BIOGEN IDEC INC

  公开号：WO2015089337A1

  公开（公告）日：2015-06-18

  The present invention provides compounds and compositions thereof which are useful as inhibitors of Bruton's tyrosine kinase and which exhibit desirable characteristics for the same.

  本发明提供了作为布鲁顿酪氨酸激酶抑制剂并具有相同理想特性的化合物及其组合物。
• Process for Preparing Tetrahydropyran-4-Carboxylic Acid Compound
  申请人：Nishino Shigeyoshi

  公开号：US20080306287A1

  公开（公告）日：2008-12-11

  The present invention is to provide a process for preparing tetrahydropyran-4-carboxylic acid represented by the formula (1): which comprises hydrolyzing a 4-cyanotetrahydropyran-4-carboxylic acid compound represented by the formula (2): wherein R represents a hydrogen atom or a hydrocarbon group, in the presence of an acid; a process for preparing a tetrahydropyran-4-carboxylic acid ester which comprises reacting the tetrahydropyran-4-carboxylic acid represented by the above-mentioned formula (1) with an alcohol in the presence of an acid; and a process for preparing tetrahydropyran-4-carboxylic acid amide which comprises reacting the tetrahydropyran-4-carboxylic acid represented by the above-mentioned formula (1) with a halogenating agent to prepare tetrahydropyran-4-carboxylic acid halide, and then, reacting an amine compound to the resulting compound.

  本发明提供了一种制备式（1）所代表的四氢吡喃-4-羧酸的过程，其包括在酸的存在下水解式（2）所代表的4-氰基四氢吡喃-4-羧酸化合物：其中R代表氢原子或烃基；一种制备四氢吡喃-4-羧酸酯的过程，其包括在酸的存在下将上述式（1）所代表的四氢吡喃-4-羧酸与醇反应；以及一种制备四氢吡喃-4-羧酸酰胺的过程，其包括将上述式（1）所代表的四氢吡喃-4-羧酸与卤化试剂反应制备四氢吡喃-4-羧酸卤化物，然后将胺化合物与所得化合物反应。
• [EN] PHARMACEUTICAL COMPOUNDS WITH SEROTONIN RECEPTOR ACTIVITY<br/>[FR] COMPOSES PHARMACEUTIQUES A ACTIVITE DE RECEPTEUR DE SEROTONINE
  申请人：LILLY CO ELI

  公开号：WO2003006455A1

  公开（公告）日：2003-01-23

  This invention relates to compounds of formula (I) wherein R2 to R10, -X-Y-, A, -W-, n and p have the values defined in claim 1, their preparation and use as pharmaceuticals.

  本发明涉及式（I）的化合物，其中R2到R10，-X-Y-，A，-W-，n和p具有权利要求书中定义的值，其制备方法以及作为药物的用途。
• Benzisothiazoles useful for treating or preventing HCV infection
  申请人：Hong Hui

  公开号：US20060229294A1

  公开（公告）日：2006-10-12

  The present invention relates to benzisothiazoles and pharmaceutical compositions thereof that inhibit replication and/or proliferation of HCV virus. The present invention also relates to the use of the benzisothiazoles and pharmaceutical compositions comprising the compounds to treat or prevent HCV infections.

  本发明涉及苯并异噻唑及其制备的制药组合物，可抑制HCV病毒的复制和/或增殖。本发明还涉及使用苯并异噻唑和包含该化合物的制药组合物来治疗或预防HCV感染。