N-Cyclopropylmethylthiourea | 618913-44-3

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫脲类
• 英文名称: N-Cyclopropylmethylthiourea
• 英文别名: cyclopropylmethylthiourea
• CAS: 618913-44-3
• 化学式: C₅H₁₀N₂S
• mdl: MFCD00276905
• 分子量: 130.21
• InChiKey: BHJTYNJTDMRWOT-UHFFFAOYSA-N

物化性质

• 熔点：
  110-113

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  8
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.8
• 拓扑面积：
  70.1
• 氢给体数：
  2
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  N-Cyclopropylmethylthiourea 、 sodium methylate 、 氰乙酸乙酯 在 溶剂黄146 、 乙醇 作用下， 以 乙醇 为溶剂， 反应 2.75h， 以giving the title compound (0.51 g, 56%)的产率得到6-amino-1-cyclopropylmethyl-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one
  参考文献：
  名称：

  Thioxanthine derivatives as myeloperoxidase inhibitors

  摘要：

  本发明揭示了使用式(Ia)或(Ib)化合物及其药学上可接受的盐，在制备药物时用于治疗或预防通过抑制酶髓过氧化物酶(MPO)有益的疾病或症状。本发明还揭示了某些新颖的式(Ia)或(Ib)化合物及其药学上可接受的盐，以及制备它们的工艺。式(Ia)和(Ib)化合物是MPO抑制剂，因此在治疗或预防神经炎症性疾病方面特别有用。

  公开号：

  US07425560B2

文献信息

• 6-Substituted-2,3,4,5-Tetrahydro-1H-Benzo[d]Azepines as 5-Ht2c Receptor Agonists
  申请人：Allen John Gordon

  公开号：US20080255092A1

  公开（公告）日：2008-10-16

  The present invention provides 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines of Formula (I) as selective 5-HT2C receptor agonists for the treatment of 5-HT2c associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety: R6 D R?N—R″R* where R6 is —(CrC3)alkyl-S—(C0-C3)alkyl-R10, —(C1-C3)alkyl-NR11R12, —(CrC3)alkyl-O—R13. and other substituents are as defined in the specification.

  本发明提供了公式（I）的6-取代的2,3,4,5-四氢-1H-苯并[d]氮杂环化合物，作为选择性5-HT2C受体激动剂，用于治疗5-HT2C相关疾病，包括肥胖症、强迫症、抑郁症和焦虑症：R6为—（CrC3）烷基-S—（C0-C3）烷基-R10，—（C1-C3）烷基-NR11R12，—（CrC3）烷基-O—R13，其他取代基如规范中所定义。
• 6-Arylalkylamino-2,3,4,5-Tetrahydro-1H-Benzo[D]Azepines as 5-Ht2c Receptor Agonists
  申请人：Briner Karin

  公开号：US20080269196A1

  公开（公告）日：2008-10-30

  The present invention provides 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines of Formula (I) as selective 5-HT2c receptor agonists for the treatment of 5-HT2c associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety, where, R6 is —NR10R11, where R10 is substituted phenylalkyl or substituted pyridylalkyl and other substituents are as defined in the specification.

  本发明提供了式（I）的6-取代的2,3,4,5-四氢-1H-苯并[d]氮杂环化合物，作为选择性5-HT2c受体激动剂，用于治疗与5-HT2c相关的疾病，包括肥胖、强迫症/强迫性障碍、抑郁症和焦虑症，其中，R6为—NR10R11，其中R10为取代的苯基烷基或取代的吡啶基烷基，其他取代基如说明书所定义。
• Thioxanthine Derivatives as Myeloperoxidase Inhibitors
  申请人：Hanson Sverker

  公开号：US20080293748A1

  公开（公告）日：2008-11-27

  There is disclosed the use of a compound of formula (Ia) or (Ib) wherein R 1 , R 2 , R 3 , R 4 , X and Y are as defined in the specification, and pharmaceutically acceptable salts thereof, in the manufacture of a medicament, for the treatment or prophylaxis of diseases or conditions in which inhibition of the enzyme myeloperoxidase (MPO) is beneficial. Certain novel compounds of formula (Ia) or (Ib) and pharmaceutically acceptable salts thereof are disclosed, together with processes for their preparation. The compounds of formulae (Ia) and (Ib) are MPO inhibitors and are thereby particularly useful in the treatment or prophylaxis of neuroinflammatory disorders.

  本发明公开了使用式(Ia)或(Ib)的化合物及其药学上可接受的盐在制备药物时的应用，其中R1、R2、R3、R4、X和Y如规范所定义，用于治疗或预防抑制酶髓过氧化物酶(MPO)对于疾病或病情的益处。公开了某些新颖的化合物(Ia)或(Ib)及其药学上可接受的盐，以及其制备方法。式(Ia)和(Ib)的化合物是MPO抑制剂，因此在治疗或预防神经炎症性疾病方面特别有用。
• 6-substituted-2,3,4,5-tetrahydro-1H-benzo[d]azepines as 5-HT2C receptor agonists
  申请人：Eli Lilly and Company

  公开号：US07994163B2

  公开（公告）日：2011-08-09

  The present invention provides 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines of Formula (I) as selective 5-HT2C receptor agonists for the treatment of 5-HT2c associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety: R6 D R?N—R″R* where R6 is —(CrC3)alkyl-S—(C0-C3)alkyl-R10, —(C1-C3)alkyl-NR11R12, —(CrC3)alkyl-O—R13. and other substituents are as defined in the specification.

  本发明提供了式(I)的6-取代2,3,4,5-四氢-1H-苯并[d]氮杂环化合物，作为选择性5-HT2C受体激动剂，用于治疗与5-HT2c相关的疾病，包括肥胖症、强迫/强迫症、抑郁症和焦虑症：R6 D R?N—R″R*，其中R6为—(CrC3)烷基-S—(C0-C3)烷基-R10，—(C1-C3)烷基-NR11R12，—(CrC3)烷基-O—R13。其他取代基如规范中所定义。
• 6-arylalkylamino-2,3,4,5-tetrahydro-1H-benzo[d]azepines as 5-HT2C receptor agonists
  申请人：Briner Karen

  公开号：US08680091B2

  公开（公告）日：2014-03-25

  The present invention provides 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines of Formula (I) as selective 5-HT2c receptor agonists for the treatment of 5-HT2c associated disorders including obesity, obsessive/compulsive disorder, depression, and anxiety, where, R6 is —NR10R11, where R10 is substituted phenylalkyl or substituted pyridylalkyl and other substituents are as defined in the specification.

  本发明提供了式（I）的6-取代2,3,4,5-四氢-1H-苯并[d]氮杂环化合物作为选择性5-HT2c受体激动剂，用于治疗5-HT2c相关疾病，包括肥胖症、强迫症、抑郁症和焦虑症，其中，R6为-NR10R11，其中R10为取代的苯基烷基或取代的吡啶基烷基，其他取代基如规范中定义。