(3R,6S)-1-tert-butyl 3-methyl 6-methylpiperidine-1,3-dicarboxylate | 1009377-05-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: (3R,6S)-1-tert-butyl 3-methyl 6-methylpiperidine-1,3-dicarboxylate
• 英文别名: 1-tert-butyl 3-methyl 6-methylpiperidine-1,3-dicarboxylate；1-tert-butyl 3-methyl (3R,6S)-rel-6-methylpiperidine-1,3-dicarboxylate；1-O-tert-butyl 3-O-methyl (3R,6S)-6-methylpiperidine-1,3-dicarboxylate
• CAS: 1009377-05-2
• 化学式: C₁₃H₂₃NO₄
• 分子量: 257.33
• InChiKey: HDRXORRYMWSTTC-VHSXEESVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.85
• 拓扑面积：
  55.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (3R,6S)-1-tert-butyl 3-methyl 6-methylpiperidine-1,3-dicarboxylate 在 二异丁基氢化铝 、 盐酸 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 1.0h， 以70%的产率得到(2S,5R)-5-(羟甲基)-2-甲基哌啶-1-甲酸叔丁酯
  参考文献：
  名称：

  MULTIMEDIATOR TRANSPORTER INHIBITORS FOR USE IN TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS

  摘要：

  该发明提供了一类抑制剂，包括这些抑制剂的包装药品，以及在治疗中枢神经系统疾病，包括抑郁症、焦虑症、睡眠障碍、肥胖症、注意力缺陷障碍（ADD）、注意力缺陷多动障碍（ADHD）、性功能障碍、物质滥用和运动障碍方面使用这些抑制剂的用途。还提供了相关的商业方法，例如进行药品业务的方法和进行医疗援助报销计划的方法。

  公开号：

  US20100093706A1
• 作为产物：
  描述：

  methyl 6-methylpiperidine-3-carboxylate 在 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 8.0h， 生成 (3R,6S)-1-tert-butyl 3-methyl 6-methylpiperidine-1,3-dicarboxylate
  参考文献：
  名称：

  CN115925615

  摘要：

  公开号：

文献信息

• NITROGEN-CONTAINING SATURATED HETEROCYCLIC COMPOUND
  申请人：SUMITOMO CHEMICAL COMPANY, LIMITED

  公开号：US20160221948A1

  公开（公告）日：2016-08-04

  The present invention provides a compound represented by the following formula (I) or its pharmaceutically acceptable salt: [wherein, R 1 represents optionally substituted C 1-4 alkyl, n shows integer of 1 to 4, R 2 represents optionally substituted C 1-4 alkyl or hydrogen atom, R 3 represents optionally substituted C 1-4 alkyl, R 4a , R 4b , R 4c , and R 4d , similarly or differently, represent optionally substituted C 6-14 aryl, optionally substituted C 1-4 alkyl, or hydrogen atom and the like, A represents optionally substituted C 6-14 aryl or optionally substituted 5 to 11 membered heteroaryl].

  本发明提供了一种由下式(I)表示的化合物或其药用可接受的盐： [其中，R1表示可选地取代的C1-4烷基，n表示1到4的整数，R2表示可选地取代的C1-4烷基或氢原子，R3表示可选地取代的C1-4烷基，R4a、R4b、R4c和R4d，相同或不同，表示可选地取代的C6-14芳基，可选地取代的C1-4烷基，或氢原子等，A表示可选地取代的C6-14芳基或可选地取代的5至11成员的杂芳基]。
• [EN] COMPOUNDS AND COMPOSITIONS FOR COGNITION-ENHANCEMENT, METHODS OF MAKING, AND METHODS OF TREATING<br/>[FR] COMPOSÉS ET COMPOSITIONS POUR AMÉLIORER LA FONCTION COGNITIVE, PROCÉDÉS DE FABRICATION ET MÉTHODES DE TRAITEMENT
  申请人：MITHRIDION INC

  公开号：WO2010102218A1

  公开（公告）日：2010-09-10

  Muscarinic agonists, which are useful for stimulating muscarinic receptors and treating cognitive disorders, are provided. Methods of synthesizing such agonists also are provided. Also provided are compositions for enhancing cognitive function in subjects such as humans, the compositions comprising a muscarinic agonist or a pharmaceutically suitable form thereof. Also provided are methods of treating animals such as humans by administering such compositions.

  提供了用于刺激肌气受体并治疗认知障碍的肌气受体激动剂。还提供了合成这类激动剂的方法。还提供了用于增强人类等受试者认知功能的组合物，该组合物包括肌气受体激动剂或其药用适宜形式。还提供了通过给予这类组合物来治疗动物如人类的方法。
• [EN] 2-ALKYL PIPERIDINE MGLUR5 RECEPTOR MODULATORS<br/>[FR] MODULATEURS DU RÉCEPTEUR MGLUR5 FOURRÉS DE 2-ALKYL PIPÉRIDINES
  申请人：MERCK SHARP & DOHME

  公开号：WO2010124055A1

  公开（公告）日：2010-10-28

  The present invention is directed to 2-alkylpiperidines which are positive allosteric modulators of metabotropic glutamate receptors, particularly the mGluR5 receptor, and which are useful in the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which metabotropic glutamate receptors are involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which metabotropic glutamate receptors are involved.

  本发明涉及2-烷基哌啶类化合物，这些化合物是代谢型谷氨酸受体的正向变构调节剂，特别是mGluR5受体，可用于治疗或预防与谷氨酸功能障碍有关的神经系统和精神疾病，以及代谢型谷氨酸受体参与的疾病。该发明还涉及包含这些化合物的药物组合物，以及这些化合物和组合物在预防或治疗涉及代谢型谷氨酸受体的疾病中的用途。
• HETEROCYCLES AND USES THEREOF
  申请人：[en]KUMQUAT BIOSCIENCES INC.

  公开号：WO2024138052A1

  公开（公告）日：2024-06-27

  The present disclosure provides compounds and pharmaceutically acceptable salts thereof, and methods of using the same. The compounds and methods have a range of utilities as therapeutics, diagnostics, and research tools. In particular, the subject compositions and methods are useful for reducing signaling output of oncogenic proteins.
• MULTIMEDIATOR TRANSPORTER INHIBITORS FOR USE IN TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS
  申请人：Hauske James R.

  公开号：US20100093706A1

  公开（公告）日：2010-04-15

  The invention provides a class of inhibitors, packaged pharmaceuticals comprising such inhibitors, and uses of the inhibitors in treating, or the manufacturing medicaments for treating central nervous system disorders, including depression, anxiety, sleep disorders, obesity, attention deficit disorder (ADD), attention deficit hyperactivity disorder (ADHD), sexual dysfunction, substance abuse, and movement disorders. Related business methods, such as methods for conducting a pharmaceutical business and methods for conducting a medical assistance reimbursement program, are also provided.

  该发明提供了一类抑制剂，包括这些抑制剂的包装药品，以及在治疗中枢神经系统疾病，包括抑郁症、焦虑症、睡眠障碍、肥胖症、注意力缺陷障碍（ADD）、注意力缺陷多动障碍（ADHD）、性功能障碍、物质滥用和运动障碍方面使用这些抑制剂的用途。还提供了相关的商业方法，例如进行药品业务的方法和进行医疗援助报销计划的方法。