3-(tert-butyloxycarbonyl)-10-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole

• 分子结构分类: 有机化合物 - 有机杂环化合物 - Pyrroloazepines
• 英文名称: 3-(tert-butyloxycarbonyl)-10-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole
• 英文别名: tert-butyl 10-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate；tert-butyl 10-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indole-3-carboxylate
• 化学式: C₂₃H₃₃BN₂O₄
• 分子量: 412.337
• InChiKey: RVEQDEAWHIQQCX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  30
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.61
• 拓扑面积：
  63.8
• 氢给体数：
  1
• 氢受体数：
  4

上下游信息

• 上游原料

  中文名称	英文名称	CAS号	化学式	分子量
  ——	3-tert-butyloxycarbonyl-10-bromo-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole	405306-08-3	C17H21BrN2O2	365.27

反应信息

• 作为产物：
  描述：

  3-tert-butyloxycarbonyl-10-bromo-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole 、 三乙胺 、 频那醇硼烷 在 双三苯基磷二氯化钯 氮气 、 甲苯 、 Brine 、 magnesium sulfate 、 crude product 、 SiO2 、 正庚烷 、 二氯甲烷 、 乙醚 作用下， 以 1,4-二氧六环 为溶剂， 反应 16.25h， 以to give tert-butyl 10-(4, 4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate (1.57 g) in 93% yield的产率得到3-(tert-butyloxycarbonyl)-10-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole
  参考文献：
  名称：

  Substituted azepino[4,5b]indole derivatives

  摘要：

  本发明公开了式(I)的化合物：其中R1-R4，p和q具有规范中描述的任何值，以及其药物盐，以及包含这样的化合物或盐的药物组合物。这些化合物和盐是5-HT配体，可用于治疗哺乳动物中涉及5-HT受体活性的疾病，障碍和/或状况。这些化合物和盐特别适用于治疗中枢神经系统疾病。

  公开号：

  US06583135B2

文献信息

• Substituted azepino[4,5b]indole derivatives
  申请人：Pharmacia & UpJohn Company

  公开号：US20030220321A1

  公开（公告）日：2003-11-27

  Disclosed are compounds of Formula (I): 1 wherein R 1 -R 4 , p and q have any of the values described in the specification, as well as pharmaceutical salts thereof, and pharmaceutical compositions containing such compounds or salts. The compounds and salts are 5-HT ligands and are useful for treating diseases, disorders, and/or conditions in a mammal wherein activity of a 5-HT receptor is implicated. The compounds and salts are particularly useful for treating diseases of the central nervous system.

  本发明涉及公式（I）的化合物：其中R1-R4，p和q的任何值均如说明书所述，以及其制备的药物盐和包含这些化合物或盐的药物组合物。这些化合物和盐是5-HT配体，并且对于治疗哺乳动物中涉及5-HT受体活性的疾病，障碍和/或状况非常有用。这些化合物和盐特别适用于治疗中枢神经系统疾病。
• Substituted azepino[4,5b]indoline derivatives
  申请人：Pharmacia & UpJohn Company

  公开号：US20030225058A1

  公开（公告）日：2003-12-04

  The invention provides compounds of Formula (I): 1 wherein R 1 -R 4 , p and q have any of the values described in the specification, as well as pharmaceutical salts thereof, and pharmaceutical compositions containing such compounds or salts. The compounds and salts are 5-HT ligands and are useful for treating diseases, disorders, and/or conditions in a mammal wherein activity of a 5-HT receptor is implicated. The compounds and salts are particularly useful for treating diseases of the central nervous system.

  本发明提供了公式(I)的化合物：1其中R1-R4，p和q具有规范中描述的任何值，以及其药物盐，以及包含该类化合物或盐的药物组合物。这些化合物和盐是5-HT配体，可用于治疗哺乳动物中涉及5-HT受体活性的疾病，紊乱和/或病况。这些化合物和盐特别适用于治疗中枢神经系统疾病。
• Substituted azepino[4,5b] indoline derivatives
  申请人：——

  公开号：US20020077318A1

  公开（公告）日：2002-06-20

  The invention provides compounds of Formula (I): 1 wherein R 1 -R 4 , p and q have any of the values described in the specification, as well as pharmaceutical salts thereof, and pharmaceutical compositions containing such compounds or salts. The compounds and salts are 5-HT ligands and are useful for treating diseases, disorders, and/or conditions in a mammal wherein activity of a 5-HT receptor is implicated. The compounds and salts are particularly useful for treating diseases of the central nervous system.

  本发明提供了式（I）的化合物：其中R1-R4，p和q具有规范中描述的任何值，以及其医药盐和含有这些化合物或盐的药物组合物。这些化合物和盐是5-HT配体，并且适用于治疗哺乳动物中涉及5-HT受体活性的疾病，障碍和/或病况。这些化合物和盐特别适用于治疗中枢神经系统疾病。
• Substituted azepino[4,5b]indole derivatives
  申请人：Pharmacia & Upjohn Company

  公开号：US06583135B2

  公开（公告）日：2003-06-24

  Disclosed are compounds of Formula (I): wherein R1-R4, p and q have any of the values described in the specification, as well as pharmaceutical salts thereof, and pharmaceutical compositions containing such compounds or salts. The compounds and salts are 5-HT ligands and are useful for treating diseases, disorders, and/or conditions in a mammal wherein activity of a 5-HT receptor is implicated. The compounds and salts are particularly useful for treating diseases of the central nervous system.

  本发明公开了式(I)的化合物：其中R1-R4，p和q具有规范中描述的任何值，以及其药物盐，以及包含这样的化合物或盐的药物组合物。这些化合物和盐是5-HT配体，可用于治疗哺乳动物中涉及5-HT受体活性的疾病，障碍和/或状况。这些化合物和盐特别适用于治疗中枢神经系统疾病。
• Substituted azepino[4,5b]indoline derivatives
  申请人：Pharmacia & Upjohn Company

  公开号：US06586421B2

  公开（公告）日：2003-07-01

  The invention provides compounds of Formula (I): wherein R1-R4, p and q have any of the values described in the specification, as well as pharmaceutical salts thereof, and pharmaceutical compositions containing such compounds or salts. The compounds and salts are 5-HT ligands and are useful for treating diseases, disorders, and/or conditions in a mammal wherein activity of a 5-HT receptor is implicated. The compounds and salts are particularly useful for treating diseases of the central nervous system.

  本发明提供了式(I)的化合物：其中R1-R4，p和q具有规范中描述的任何值，以及其药物盐和含有这种化合物或盐的药物组合物。这些化合物和盐是5-HT配体，可用于治疗哺乳动物中涉及5-HT受体活性的疾病，疾患和/或情况。这些化合物和盐特别适用于治疗中枢神经系统疾病。