5-(2-iodophenyl)-3-methyl-1,2,4-oxadiazole

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 5-(2-iodophenyl)-3-methyl-1,2,4-oxadiazole
• 化学式: C₉H₇IN₂O
• mdl: MFCD21091817
• 分子量: 286.072
• InChiKey: LEIOSXBPHMHDGJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.111
• 拓扑面积：
  38.9
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  5-(2-iodophenyl)-3-methyl-1,2,4-oxadiazole 在 甲醇 、 1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物 、 三乙胺 、 sodium hydroxide 作用下， 以 二甲基亚砜 为溶剂， 生成 2-(3-甲基-1,2,4-噁二唑-5-基)苯甲酸
  参考文献：
  名称：

  [EN] PYRROLIDINE OREXIN RECEPTOR ANTAGONISTS
  [FR] COMPOSÉS PYRROLIDINE EN TANT QU'ANTAGONISTES DU RÉCEPTEUR DE L'HYPOCRÉTINE

  摘要：

  本发明涉及对促进素受体的拮抗剂吡咯烷化合物。本发明还涉及所述化合物在潜在的治疗或预防涉及促进素受体的神经和精神疾病和疾病中的用途。本发明还涉及包含这些化合物的组合物。本发明还涉及这些组合物在潜在的预防或治疗涉及促进素受体的疾病中的用途。

  公开号：

  WO2016095204A1
• 作为产物：
  描述：

  2-碘氰基苯 在 羟胺 作用下， 以 乙醇 为溶剂， 反应 1.0h， 生成 5-(2-iodophenyl)-3-methyl-1,2,4-oxadiazole
  参考文献：
  名称：

  [EN] PYRROLIDINE OREXIN RECEPTOR ANTAGONISTS
  [FR] COMPOSÉS PYRROLIDINE EN TANT QU'ANTAGONISTES DU RÉCEPTEUR DE L'HYPOCRÉTINE

  摘要：

  本发明涉及对促进素受体的拮抗剂吡咯烷化合物。本发明还涉及所述化合物在潜在的治疗或预防涉及促进素受体的神经和精神疾病和疾病中的用途。本发明还涉及包含这些化合物的组合物。本发明还涉及这些组合物在潜在的预防或治疗涉及促进素受体的疾病中的用途。

  公开号：

  WO2016095204A1

文献信息

• [EN] PYRROLIDINE OREXIN RECEPTOR ANTAGONISTS<br/>[FR] COMPOSÉS PYRROLIDINE EN TANT QU'ANTAGONISTES DU RÉCEPTEUR DE L'HYPOCRÉTINE
  申请人：MERCK SHARP & DOHME

  公开号：WO2016095204A1

  公开（公告）日：2016-06-23

  The present invention is directed to pyrrolidine compounds which are antagonists of orexin receptors. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which orexin receptors are involved.

  本发明涉及对促进素受体的拮抗剂吡咯烷化合物。本发明还涉及所述化合物在潜在的治疗或预防涉及促进素受体的神经和精神疾病和疾病中的用途。本发明还涉及包含这些化合物的组合物。本发明还涉及这些组合物在潜在的预防或治疗涉及促进素受体的疾病中的用途。
• Ethyldiamine orexin receptor antagonists
  申请人：Merck Sharp & Dohme Corp.

  公开号：US10011595B2

  公开（公告）日：2018-07-03

  The present invention is directed to ethyldiamne compounds which are antagonists of orexin receptors. Such compounds are of the general structural formula I: The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to pharmaceutical compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which orexin receptors are involved.

  本发明涉及作为奥曲肽受体拮抗剂的乙二胺化合物。此类化合物的结构通式为 I： 本发明还涉及本文所述化合物在潜在治疗或预防涉及奥曲肽受体的神经和精神疾病中的用途。本发明还涉及包含这些化合物的药物组合物。本发明还涉及这些组合物在潜在预防或治疗涉及奥曲肽受体的此类疾病中的用途。
• Pyrrolidine orexin receptor antagonists
  申请人：Merck Sharp & Dohme Corp.

  公开号：US10150751B2

  公开（公告）日：2018-12-11

  The present invention is directed to pyrrolidine compounds which are antagonists of orexin receptors. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which orexin receptors are involved.

  本发明涉及作为奥曲肽受体拮抗剂的吡咯烷化合物。本发明还涉及本文所述化合物在潜在治疗或预防涉及奥曲肽受体的神经和精神疾病中的用途。本发明还涉及包含这些化合物的组合物。本发明还涉及这些组合物在潜在预防或治疗涉及奥曲肽受体的此类疾病中的用途。
• Oxazole orexin receptor antagonists
  申请人：MERCK SHARP & DOHME CORP.

  公开号：US10435398B2

  公开（公告）日：2019-10-08

  The present invention is directed to oxazole compounds which are antagonists of orexin receptors. The present invention is also directed to uses of the oxazole compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to pharmaceutical compositions comprising these compounds. The present invention is also directed to uses of these pharmaceutical compositions in the potential prevention or treatment of such diseases in which orexin receptors are involved.

  本发明涉及奥曲肽受体拮抗剂噁唑化合物。本发明还涉及本文所述噁唑化合物在潜在治疗或预防涉及奥曲肽受体的神经和精神疾病中的用途。本发明还涉及包含这些化合物的药物组合物。本发明还涉及这些药物组合物在潜在预防或治疗涉及奥曲肽受体的此类疾病中的用途。
• 一种2-芳香胺基嘧啶类化合物及其制备方法与应用
  申请人：北京英飞智药科技有限公司

  公开号：CN117800953A

  公开（公告）日：2024-04-02

  本申请涉及生物医药技术领域，具体公开了一种2‑芳香胺基嘧啶类化合物及其制备方法与应用。本申请提供一种2‑芳香胺基嘧啶类化合物，该化合物为通式I所示的化合物或其药学上可接受的盐、异构体、溶剂化物、水合物、前药或同位素衍生物；通式I的结构式为：#imgabs0#本申请提供的2‑芳香胺基嘧啶类化合物对PLK1的活性具有很强的抑制作用，有望开发成为新型抗肿瘤药物。