6-氟-2,3,4,9-四氢-1H-咔唑-3-甲醛 | 843653-04-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 中文名称: 6-氟-2,3,4,9-四氢-1H-咔唑-3-甲醛
• 英文名称: 6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde
• CAS: 843653-04-3
• 化学式: C₁₃H₁₂FNO
• 分子量: 217.243
• InChiKey: JNWWVPWEZUZEMV-UHFFFAOYSA-N

物化性质

• 熔点：
  96-98 °C
• 沸点：
  385.0±42.0 °C(Predicted)
• 密度：
  1.362±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  16
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  32.9
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 海关编码：
  2933990090

反应信息

• 作为反应物：
  描述：

  6-氟-2,3,4,9-四氢-1H-咔唑-3-甲醛 、 [(2S)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methylamine 在 sodium cyanoborohydride 、 溶剂黄146 作用下， 以 甲醇 为溶剂， 以48%的产率得到N-[(6-fluoro-2,3,4,9-tetrahydro-1H-carbazol-3-yl)methyl]-N-{[(2S)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinoIin-2-yI]methyl}amine
  参考文献：
  名称：

  First Scale-Up: Problems and Resolutions on the Synthesis of WAY-253752, a Novel, Dual-Acting SSRI/5HT_1A Antagonist

  摘要：

  An alternative synthesis of WAY-253752, 1, a novel, dual-acting SSRI/5HT(1A) antagonist, was developed and used for the first scale-up. Initially, the target compound was synthesized as part of a diasteromeric mixture separated by chiral preparative HPLC. The new route was designed around intermediates suitable for chiral resolution, and its conditions were successfully determined.

  DOI：

  10.1021/op700181n
• 作为产物：
  描述：

  对环己酮甲酸乙酯 在 lithium aluminium tetrahydride 、 N,N'-二环己基碳二亚胺 、 三氟乙酸 作用下， 以 四氢呋喃 、 乙醇 、 二甲基亚砜 、 苯 为溶剂， 反应 16.0h， 生成 6-氟-2,3,4,9-四氢-1H-咔唑-3-甲醛
  参考文献：
  名称：

  First Scale-Up: Problems and Resolutions on the Synthesis of WAY-253752, a Novel, Dual-Acting SSRI/5HT_1A Antagonist

  摘要：

  An alternative synthesis of WAY-253752, 1, a novel, dual-acting SSRI/5HT(1A) antagonist, was developed and used for the first scale-up. Initially, the target compound was synthesized as part of a diasteromeric mixture separated by chiral preparative HPLC. The new route was designed around intermediates suitable for chiral resolution, and its conditions were successfully determined.

  DOI：

  10.1021/op700181n

文献信息

• [EN] 3-AMINO CHOMAN AND 2-AMINO TETRALIN DERIVATIVES<br/>[FR] DERIVES 3-AMINO CHOMANE ET 2-AMINO TETRALINE
  申请人：WYETH CORP

  公开号：WO2005012291A1

  公开（公告）日：2005-02-10

  3-Amino chroman and 2-amino tetralin derivatives and compositions containing such compounds are disclosed. Methods of using the 3-amino chroman and 2-amino tetralin compounds and compositions containing such compounds in the treatment of serotonin disorders, such as depression and anxiety, are also disclosed.

  揭示了3-氨基色苷和2-氨基四氢萘衍生物以及含有这些化合物的组合物。还揭示了在治疗血清素失调症，如抑郁症和焦虑症中使用3-氨基色苷和2-氨基四氢萘化合物以及含有这些化合物的组合物的方法。
• 3-Amino chroman and 2-amino tetralin derivatives
  申请人：Hatzenbuhler Theriault Nicole

  公开号：US20050032873A1

  公开（公告）日：2005-02-10

  3-Amino chroman and 2-amino tetralin derivatives and compositions containing such compounds are disclosed. Methods of using the 3-amino chroman and 2-amino tetralin compounds and compositions containing such compounds in the treatment of serotonin disorders, such as depression and anxiety, are also disclosed.

  本文披露了3-氨基色满和2-氨基四氢萘衍生物及含有这些化合物的组合物。还披露了使用3-氨基色满和2-氨基四氢萘化合物及含有这些化合物的组合物治疗血清素失调症，如抑郁和焦虑的方法。
• Cycloalkylfused indole, benzothiophene, benzofuran and indene derivatives
  申请人：Sabb Louise Annmarie

  公开号：US20060205759A1

  公开（公告）日：2006-09-14

  The present invention provides cycloalkylfused indole, benzothiophene, benzofuran, and indene derivatives, and methods for using them to, for example, treat, prevent and/or ameliorate central nervous system diseases by antagonizing 5-HT 1A receptors and modulating serotonin levels.

  本发明提供环烷基融合吲哚、苯并噻吩、苯并呋喃和茚烯衍生物，以及使用它们的方法，例如通过拮抗5-HT1A受体和调节血清素水平来治疗、预防和/或改善中枢神经系统疾病。
• CYCLOALKYLFUSED INDOLE, BENZOTHIOPHENE, BENZOFURAN AND INDENE DERIVATIVES
  申请人：Sabb Louise Annmarie

  公开号：US20080081910A1

  公开（公告）日：2008-04-03

  The present invention provides cycloalkylfused indole, benzothiophene, benzofuran, and indene derivatives, and methods for using them to, for example, treat, prevent and/or ameliorate central nervous system diseases by antagonizing 5-HT 1A receptors and modulating serotonin levels.

  本发明提供了环烷基融合吲哚、苯并噻吩、苯并呋喃和茚烯衍生物，以及使用它们的方法，例如通过拮抗5-HT1A受体和调节血清素水平来治疗、预防和/或改善中枢神经系统疾病。
• Compounds useful as serotonin inhibitors and 5-HT1A agonists and antagonists
  申请人：Ramamoorthy Sivaramakrishnan P.

  公开号：US20070149585A1

  公开（公告）日：2007-06-28

  3-Amino chroman and 2-amino tetralin derivatives and compositions containing such compounds are disclosed. Such compounds are useful for modulating activity of a 5-HT 1A receptor (agonizing or antagonizing) in a patient. These compounds are further useful for inhibiting binding to a serotonin receptor. Methods of using the 3-amino chroman and 2-amino tetralin compounds and compositions containing such compounds in the treatment of serotonin disorders, such as depression and anxiety, are also disclosed.

  本发明涉及3-氨基色基和2-氨基四氢萘衍生物以及含有这种化合物的组合物。这些化合物对于调节患者的5-HT1A受体的活性（激动或拮抗）非常有用。这些化合物还对于抑制与5-羟色胺受体的结合也非常有用。本发明还公开了使用3-氨基色基和2-氨基四氢萘化合物以及含有这种化合物的组合物治疗5-羟色胺失调如抑郁和焦虑的方法。