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3-(5-氟-1H-吲哚-3-基)丙胺 | 245762-27-0

中文名称
3-(5-氟-1H-吲哚-3-基)丙胺
中文别名
3-(5-氟-3-吲哚基)-1-丙胺
英文名称
3-(5-fluoro-1H-indol-3-yl)-propylamine
英文别名
3-(5-fluoro-3-indolyl)propylamine;3-(propyl-3-amine)-5-fluoro-1H-indole;3-(3-aminopropyl)-5-fluoro-1H-indole;3-(5-fluoro-1H-indol-3-yl)propan-1-amine
3-(5-氟-1H-吲哚-3-基)丙胺化学式
CAS
245762-27-0
化学式
C11H13FN2
mdl
MFCD04966926
分子量
192.236
InChiKey
JBFFCANWDYAYFN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    82-84.5 °C
  • 沸点:
    357.2±32.0 °C(Predicted)
  • 密度:
    1.208±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.272
  • 拓扑面积:
    41.8
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:1821ec20d09fadeba2bd608fa0d65933
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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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2

反应信息

  • 作为反应物:
    描述:
    3-(5-氟-1H-吲哚-3-基)丙胺 在 palladium on activated charcoal 氢气三乙胺 作用下, 以 乙醇二甲基亚砜 为溶剂, 反应 15.0h, 生成 3-{2-[3-(5-fluoro-1H-indol-3-yl)propylamino]ethoxy}benzene-1,2-diamine
    参考文献:
    名称:
    Studies toward the Discovery of the Next Generation of Antidepressants. 3. Dual 5-HT1A and Serotonin Transporter Affinity within a Class of N-Aryloxyethylindolylalkylamines
    摘要:
    N-Aryloxylethylindolealkylamines (5) having dual 5-HT transporter and 5-HT1A affinity are described. These compounds represent truncated analogues of our previously reported piperidinyl derivatives (3). Compounds in this investigation were found to have more similar affinities and functional activities for the 5-HT1A receptor and 5-HT transporter. Though 5-HT1A antagonism is not consistently observed throughout series 5, several molecular features were found to be essential to obtain high and balanced activities. The proper placement of a heteroatom in the aryl ring and the length of the linkage used to tether the indole moiety had significant influence on 5-HT1A and 5-HT transporter affinities. Introduction of a halogen into the aryl ring usually lowered intrinsic activity and in some cases led to full 5-HT1A antagonists. Compounds 33 and 34 were observed to be full 5-HT1A antagonists with K-i values of approximately 30 nM for the 5-HT1A receptor and K-i values of 5 and 0.5 nM for the 5-HT transporter, respectively. Unfortunately, similar to our previous series (3), compounds in this report also had high affinity for the alpha(1) receptor.
    DOI:
    10.1021/jm0304010
  • 作为产物:
    描述:
    3-(3-溴丙基)-5-氟-1H-吲哚 在 palladium on activated charcoal sodium azide 、 氢气 作用下, 以 乙醇N,N-二甲基甲酰胺 为溶剂, 60.0 ℃ 、344.74 kPa 条件下, 反应 34.0h, 生成 3-(5-氟-1H-吲哚-3-基)丙胺
    参考文献:
    名称:
    Studies toward the Discovery of the Next Generation of Antidepressants. 3. Dual 5-HT1A and Serotonin Transporter Affinity within a Class of N-Aryloxyethylindolylalkylamines
    摘要:
    N-Aryloxylethylindolealkylamines (5) having dual 5-HT transporter and 5-HT1A affinity are described. These compounds represent truncated analogues of our previously reported piperidinyl derivatives (3). Compounds in this investigation were found to have more similar affinities and functional activities for the 5-HT1A receptor and 5-HT transporter. Though 5-HT1A antagonism is not consistently observed throughout series 5, several molecular features were found to be essential to obtain high and balanced activities. The proper placement of a heteroatom in the aryl ring and the length of the linkage used to tether the indole moiety had significant influence on 5-HT1A and 5-HT transporter affinities. Introduction of a halogen into the aryl ring usually lowered intrinsic activity and in some cases led to full 5-HT1A antagonists. Compounds 33 and 34 were observed to be full 5-HT1A antagonists with K-i values of approximately 30 nM for the 5-HT1A receptor and K-i values of 5 and 0.5 nM for the 5-HT transporter, respectively. Unfortunately, similar to our previous series (3), compounds in this report also had high affinity for the alpha(1) receptor.
    DOI:
    10.1021/jm0304010
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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。
  • N-aryloxyethyl-indoly-alkylamines for the treatment of depression
    申请人:American Home Products Corp.
    公开号:US06121307A1
    公开(公告)日:2000-09-19
    Compounds useful for alleviating symptoms of depression are provided which have the following formula: wherein: R.sub.1 is hydrogen, lower alkyl or aryl; R.sub.2 is hydrogen, lower alkyl, phenyl or substituted phenyl; X and Y are each, independently, hydrogen, lower alkyl, lower alkoxy, or halogen, or together combine with the carbon atoms to which they are attached to complete a pyranyl, dihydrofuranyl, furanyl, or dioxanyl, group; Z is hydrogen, halogen or lower alkoxy; with the proviso that when X, Y or Z represent lower alkoxy, they are not present at the ortho position; W is hydrogen, halogen, lower alkyl, cyano or a trifluoromethyl group; and n is 2-5; or pharmaceutically acceptable salts thereof.
    提供了用于缓解抑郁症症状的化合物,其具有以下结构式:其中:R.sub.1为氢、低碳基或芳基;R.sub.2为氢、低碳基、苯基或取代苯基;X和Y分别独立地为氢、低碳基、低烷氧基或卤素,或者与它们连接的碳原子结合在一起形成吡喃基、二氢呋喃基、呋喃基或二氧杂环基;Z为氢、卤素或低烷氧基;但当X、Y或Z代表低烷氧基时,它们不位于邻位;W为氢、卤素、低碳基、氰基或三氟甲基基团;n为2-5;或其药用盐。
  • [EN] ANTIDEPRESSANT INDOLEALKYL DERIVATIVES OF HETEROCYCLE-FUSED BENZODIOXAN METHYLAMINES<br/>[FR] DERIVES INDOLEALKYLE D'HETEROCYCLE DE BENZODIOXAN FUSIONNES METHYLAMINES EN TANT QU'ANTIDEPRESSEURS
    申请人:WYETH CORP
    公开号:WO2004024734A1
    公开(公告)日:2004-03-25
    Compounds of the Formula: are useful for the treatment of depression ( including but not limited to major depressive disorder, childhood depression and dysthymia). Anxiety, panic disorder, post-traumatic stress disorder, premenstrual dysphoric disorder (also known as premenstrual syndrome), attention deficit disorder ( with and without hyperactivity), obsessive compulsive disorder, social anxiety disorder, generalized anxiety disorder, obesity, eating disorders such as anorexia nervosa, bulimia nervosa, vasomotor flushing, cocaine and alcohol addiction, sexual dysfunction and related illnesses.
    这个公式的化合物对治疗抑郁症(包括但不限于重性抑郁障碍、儿童抑郁症和慢性抑郁症)非常有用。焦虑、恐慌障碍、创伤后应激障碍、经前期失调性障碍(也称为经前综合征)、注意力缺陷障碍(伴有或不伴有多动症)、强迫症、社交焦虑障碍、广泛性焦虑障碍、肥胖、厌食症、暴食症、血管运动性潮红、可卡因和酒精成瘾、性功能障碍及相关疾病均有一定疗效。
  • 3,4-Dihydro-2H-benzo&lsqb;1,4&rsqb;oxazinyl-methyl)-&lsqb;3-(1H-indol-3yl)-alkyl&rsqb;- amines
    申请人:American Home Products Corp
    公开号:US06313114B1
    公开(公告)日:2001-11-06
    Compounds are provided which have the following formula: wherein: R is hydrogen, alkyl of 1 to 6 carbon atoms, phenyl, or substituted phenyl; X and Y are each, independently, hydrogen, halogen, cyano, or alkoxy of 1 to 6 carbon atoms; and m is 1 to 5; or a pharmaceutically acceptable salt thereof.
    提供具有以下化学式的化合物:其中:R为氢、1至6个碳原子的烷基、苯基或取代苯基;X和Y分别独立地为氢、卤素、氰基或1至6个碳原子的烷氧基;m为1至5;或其药用可接受盐。
  • Hypervalent Iodine-Mediated Cyclization of Homotryptamine Derivatives
    作者:Xinpeng Jiang、Weijie Zhu、Liechao Yang、Zicong Zheng、Chuanming Yu
    DOI:10.1002/ejoc.201801842
    日期:2019.3.31
    A facile and efficient cyclization of homotryptamines and their derivatives has been established for the construction of 4a‐chlorotetrahydropyrido[2,3‐b]indoles and 3,3‐spirocyclic 3H‐indoles using hypervalent iodine (1‐chloro‐1,2‐benziodoxol‐3‐one) under mild conditions. The broad substrate scope and successful gram‐scale experiment grant this metal‐free transformation great potential for further
    已经建立了使用高价碘(1-氯-1,2-二甲基吡啶)构建4a-氯四氢吡啶并[2,3-b]吲哚和3,3-螺环3 H-吲哚的简便高效的环类胺及其衍生物的环化方法。苯并三唑-3-酮)在温和的条件下使用。广泛的基体范围和成功的克级实验为这种无金属的转化提供了进一步应用的巨大潜力。
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