(S)-1-pyrrolidin-1-yl-butan-2-ol | 1104082-45-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: (S)-1-pyrrolidin-1-yl-butan-2-ol
• 英文别名: (2S)-1-pyrrolidin-1-ylbutan-2-ol
• CAS: 1104082-45-2
• 化学式: C₈H₁₇NO
• 分子量: 143.229
• InChiKey: FJRHRYPEAFRRON-QMMMGPOBSA-N

物化性质

• 沸点：
  219.4±13.0 °C(Predicted)
• 密度：
  0.966±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  10
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  23.5
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  (S)-1-pyrrolidin-1-yl-butan-2-ol 、 tert-butyl 4-(3-fluoropyrazin-2-yl)piperidine-1-carboxylate 在 sodium hydride 、 水 、 氯化铵 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 2.0h， 生成
  参考文献：
  名称：

  Substituted heteroarylpiperidine derivatives as melanocortin-4 receptor modulators

  摘要：

  本发明涉及取代杂环基哌啶衍生物作为黑色素皮质素-4受体调节剂。根据该发明的化合物的结构和立体化学，这些化合物要么是人类黑色素皮质素-4受体（MC-4R）的选择性激动剂，要么是选择性拮抗剂。激动剂可用于治疗肥胖、糖尿病和性功能障碍等疾病和疾病，而拮抗剂可用于治疗癌症恶病质、肌肉萎缩、厌食症、焦虑和抑郁等疾病和疾病。通常，所有涉及MC-4R调节的疾病和疾病均可使用本发明的化合物进行治疗。

  公开号：

  EP2019100A1
• 作为产物：
  描述：

  四氢吡咯 、 (S)-(-)-1,2-环氧丁烷 在 乙醚 、 Sodium sulfate-III 、 甲苯 作用下， 以 水 为溶剂， 反应 16.0h， 生成 (S)-1-pyrrolidin-1-yl-butan-2-ol
  参考文献：
  名称：

  Substituted Heteroarylpiperidine Derivatives As Melanocortin-4 Receptor Modulators

  摘要：

  本发明涉及取代杂环基哌啶衍生物作为黑色素-4受体调节剂。根据化合物的结构和立体化学，本发明的化合物可以是人类黑色素-4受体（MC-4R）的选择性激动剂或选择性拮抗剂。激动剂可用于治疗肥胖症、糖尿病和性功能障碍等疾病和疾病，而拮抗剂可用于治疗癌症消耗症、肌肉萎缩、厌食症、肌萎缩侧索硬化症（ALS）、焦虑和抑郁症等疾病和疾病。通常，涉及MC-4R调节的所有疾病和疾病都可以用本发明的化合物治疗。

  公开号：

  US20100249093A1

文献信息

• SUBSTITUTED HETEROARYLPIPERIDINE DERIVATIVES AS MELANOCORTIN-4 RECEPTOR MODULATORS
  申请人：Santhera Pharmaceuticals (Schweiz) AG

  公开号：EP2176250A1

  公开（公告）日：2010-04-21
• Isoxazole Carboxamide Compounds
  申请人：EPIZYME, INC.

  公开号：US20170190676A1

  公开（公告）日：2017-07-06

  The present disclosure provides substituted isoxazole carboxamide compounds having Formula (I) and the pharmaceutically acceptable salts and solvates thereof, wherein R 1 , R 2 , A, X, and Z are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula I to treat a disorder responsive to the blockade of SMYD proteins such as SMYD3 or SMYD2. Compounds of the present disclosure are especially useful for treating cancer.
• SMYD Inhibitors
  申请人：EPIZYME, INC.

  公开号：US20170355695A1

  公开（公告）日：2017-12-14

  The present disclosure provides carboxamides and sulfonamides having Formula (I): and the pharmaceutically acceptable salts and solvates thereof, wherein A, Y, B, X, and Z are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of SMYD proteins such as SMYD3 or SMYD2. Compounds of the present disclosure are especially useful for treating cancer.
• SMYD INHIBITORS
  申请人：EPIZYME, INC.

  公开号：US20210198252A1

  公开（公告）日：2021-07-01

  The present disclosure provides carboxamides and sulfonamides having Formula (I): and the pharmaceutically acceptable salts and solvates thereof, wherein A, Y, B, X, and Z are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula (I) to treat a disorder responsive to the blockade of SMYD proteins such a SMYD3 or SMYD2. Compounds of the present disclosure are especially useful for treating cancer.
• [EN] SUBSTITUTED HETEROARYLPIPERIDINE DERIVATIVES AS MELANOCORTIN-4 RECEPTOR MODULATORS<br/>[FR] DÉRIVÉS D'HÉTÉROARYLPIPÉRIDINE SUBSTITUÉS UTILISÉS COMME MODULATEURS DU RÉCEPTEUR 4 DE LA MÉLANOCORTINE
  申请人：SANTHERA PHARMACEUTICALS CH

  公开号：WO2009010299A1

  公开（公告）日：2009-01-22

  The present invention relates to substituted heteroarylpiperidine derivative (I) as melanocortin-4 receptor modulators. Depending on the structure and the stereochemistry the compounds of the invention are either selective agonists or selective antagonists of the human melanocortin-4 receptor (MC-4R). The agonists can be used for the treatment of disorders and diseases such as obesity, diabetes and sexual dysfunction, whereas the antagonists are useful for the treatment of disorders and diseases such as cancer cachexia, muscle wasting, anorexia, amyotrophic lateral sclerosis (ALS), anxiety and depression. Generally all diseases and disorders where the regulation of the MC-4R is involved can be treated with the compounds of the invention.