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N-benzo[b]thien-3-yl-N-(4-pyridyl)amine | 165107-36-8

中文名称
——
中文别名
——
英文名称
N-benzo[b]thien-3-yl-N-(4-pyridyl)amine
英文别名
3-(4-pyridinylamino)benzo[b]thiophene;N-(1-benzothiophen-3-yl)pyridin-4-amine
N-benzo[b]thien-3-yl-N-(4-pyridyl)amine化学式
CAS
165107-36-8
化学式
C13H10N2S
mdl
——
分子量
226.302
InChiKey
MQYXOPRBMSZZQV-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

  • 沸点:
    429.9±20.0 °C(Predicted)
  • 密度:
    1.313±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    53.2
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    N-benzo[b]thien-3-yl-N-(4-pyridyl)amine硫酸二甲酯 作用下, 以 N-甲基乙酰胺甲醇 、 (2S)-N-methyl-1-phenylpropan-2-amine hydrate 为溶剂, 生成 3-(Methyl-4-pyridinylamino)benzo[b]thiophene hydrochloride
    参考文献:
    名称:
    Substituted (pyridinylamino)-indoles
    摘要:
    下面公式中披露了各种化合物,##STR1## 其中R、R.sub.1、W、X、Y和Z的定义如规范中所述;这些化合物对于缓解各种记忆功能障碍(如阿尔茨海默病)、作为神经递质功能的调节剂(如5-羟色胺和肾上腺素),以及作为抗抑郁药、抗焦虑药、非典型抗精神病药、止吐药,以及用于治疗强迫性障碍等人格障碍方面是有用的。
    公开号:
    US05328920A1
  • 作为产物:
    描述:
    4-氨基吡啶3-溴苯并噻吩caesium carbonate4,5-双二苯基膦-9,9-二甲基氧杂蒽 、 bis(dibenzylideneacetone)-palladium(0) 作用下, 以 甲苯 为溶剂, 反应 24.0h, 以36%的产率得到N-benzo[b]thien-3-yl-N-(4-pyridyl)amine
    参考文献:
    名称:
    钯催化的多米诺Ç ?H / N ?H功能化:氮桥杂蒽的有效方法
    摘要:
    钯催化的多米诺Ç  H /Ñ  ħ官能新型含氮桥连thienoacenes的合成和10 ħ -苯并[4,5]噻吩并[3,2- b ]报道从二卤代芳烃吲哚衍生物。该多米诺序列由苯并[ b ]噻吩部分的初始CH功能化,然后是布赫瓦尔德-哈特维格偶联。这种转变对于合成高度π扩展的化合物也很有用。
    DOI:
    10.1002/chem.201500897
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文献信息

  • Interleukin-4 gene expression inhibitors
    申请人:——
    公开号:US20040006123A1
    公开(公告)日:2004-01-08
    This invention discloses and claims a class of indole and benzo(b)thiophene derivatives for use in treating allergy, asthma, rhinitis, dermatitis, B-cell lymphomas, tumors and diseases associated with bacterial, rhinovirus or respiratory syncytial virus (RSV) infections. The compounds of this invention are defined by the Formula (I): 1 wherein X, Y, Z, R 1 , R 2 and R 3 are as defined in the specification; or a pharmaceutically acceptable salt thereof. In preferred embodiments of this invention it is also disclosed and claimed that the compounds of this invention are capable of modulating T helper (Th) cells, Th1/Th2, and thereby capable of inhibiting the transcription of interleukin-4 (IL-4) message, IL-4 release or IL-4 production.
    这项发明揭示并声明了一类吲哚和苯并(b)噻吩衍生物,用于治疗过敏、哮喘、鼻炎、皮炎、B细胞淋巴瘤、肿瘤以及与细菌、鼻病毒或呼吸道合胞病毒(RSV)感染相关的疾病。本发明的化合物由下式(I)定义: 1 其中X、Y、Z、R 1 、R 2 和R 3 如规范中所定义;或其药学上可接受的盐。在本发明的优选实施例中,还揭示并声明了本发明的化合物能够调节T辅助(Th)细胞、Th1/Th2,从而能够抑制白细胞介素-4(IL-4)信息的转录、IL-4的释放或IL-4的产生。
  • Indole derivatives as interleukin -4 gene expression inhibitors
    申请人:——
    公开号:US20040010029A1
    公开(公告)日:2004-01-15
    This invention discloses and claims a new class of indole derivatives for use in treating allergy, asthma, rhinitis, dermatitis, B-cell lymphomas, tumors and diseases associated with bacterial, rhinovirus or respiratory syncytial virus (RSV) infections. It has now been found that the compounds of this invention are capable of modulating T helper (Th) cells, Th1/Th2, and thereby capable of inhibiting the transcription of interleukin-4 (IL-4) message, IL-4 release or IL-4 production.
    这项发明揭示并声明了一类新的吲哚衍生物,用于治疗过敏、哮喘、鼻炎、皮炎、B细胞淋巴瘤、肿瘤以及与细菌、鼻病毒或呼吸道合胞病毒(RSV)感染相关的疾病。现在已经发现,该发明的化合物能够调节T辅助细胞(Th)细胞、Th1 / Th2,从而能够抑制白细胞介素-4(IL-4)信息的转录、IL-4释放或IL-4的产生。
  • INTERLEUKIN-4 GENE EXPRESSION INHIBITORS
    申请人:ALKAN Sefik S.
    公开号:US20080132481A1
    公开(公告)日:2008-06-05
    This invention discloses and claims a class of indole and benzo(b)thiophene derivatives for use in treating allergy, asthma, rhinitis, dermatitis, B-cell lymphomas, tumors and diseases associated with bacterial, rhinovirus or respiratory syncytial virus (RSV) infections. The compounds of this invention are defined by the Formula (I): wherein X, Y, Z, R 1 , R 2 and R 3 are as defined in the specification; or a pharmaceutically acceptable salt thereof. In preferred embodiments of this invention it is also disclosed and claimed that the compounds of this invention are capable of modulating T helper (Th) cells, Th1/Th2, and thereby capable of inhibiting the transcription of interleukin-4 (IL-4) message, IL-4 release or IL-4 production.
    本发明揭示和声明了一类用于治疗过敏、哮喘、鼻炎、皮炎、B细胞淋巴瘤、肿瘤以及与细菌、鼻病毒或呼吸道合胞病毒(RSV)感染相关的疾病的吲哚和苯并(b)噻吩衍生物。本发明的化合物由公式(I)定义:其中X、Y、Z、R1、R2和R3如规范中所定义;或其药学上可接受的盐。在本发明的优选实施例中,还揭示和声明本发明的化合物能够调节T辅助(Th)细胞,Th1 / Th2,并能够抑制白细胞介素-4(IL-4)信息的转录、IL-4的释放或IL-4的产生。
  • Substituted 3-(Pyridinylamino)-indoles and benzo[b]thiophenes, a process for their preparation and their use as medicaments
    申请人:HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED
    公开号:EP0509402A1
    公开(公告)日:1992-10-21
    The present invention relates to compounds of the formula I where R₁is hydrogen, loweralkyl, loweralkenyl, loweralkynyl, arylloweralkyl, aminoloweralkyl, loweralkylaminoloweralkyl, formyl, loweralkylcarbonyl, aminoloweralkylcarbonyl or loweralkoxycarbonyl; the group -X-Y= is R₂ and R₃ being independently hydrogen or loweralkyl; Wis hydrogen, halogen, hydroxy, loweralkoxy, arylloweralkoxy or where R₄ is hydrogen, loweralkyl or arylloweralkyl; R₅ is loweralkyl or arylloweralkyl; or alternatively the group as a whole is , R₆ being hydrogen, loweralkyl, aryl or arylloweralkyl; and Zis hydrogen, halogen, loweralkyl, nitro or amino; which are useful for alleviating various memory dysfunctions such as Alzheimer's disease, as modulators of neurotransmitter functions such as serotonergic and adrenergic, and as such are useful as antidepressants, anxiolytics, atypical antipsychotics, antiemetics, and for the treatment of personality disorders such as obsessive compulsive disorders.
    本发明涉及式 I 的化合物 式中 R₁是氢、低级烷基、低级烯基、低级炔基、芳基低级烷基、氨基低级烷基、氨基低级烷基、甲酰基、低级烷基羰基、氨基低级烷基羰基或低级烷氧基羰基; 基团 -X-Y= 是 R₂ 和 R₃ 独立为氢或低级烷基; 是氢、卤素、羟基、低级烷氧基、芳基低级烷氧基或 其中 R₄ 是氢、低级烷基或芳基低级烷基; R₅ 是低级烷基或芳基低级烷基;或者,该基团 作为一个整体是 R₆ 是氢、低级烷基、芳基或芳基低级烷基;以及 Z 是氢、卤素、低级烷基、硝基或氨基; 这些物质可用于缓解各种记忆功能障碍,如阿尔茨海默氏症,作为神经递质功能的调节剂,如血清素能和肾上腺素能,因此可用作抗抑郁药、抗焦虑药、非典型抗精神病药、止吐药,以及用于治疗人格障碍,如强迫症。
  • 3-substituted amino-1H-indole-2-carboxylic acid and 3-substituted amino-benzo[B]thiophene-2carboxylic acid derivatives as interleukin-4 gene expression inhibitors
    申请人:Aventis Pharmaceuticals Inc.
    公开号:EP1834947A2
    公开(公告)日:2007-09-19
    This invention discloses and claims a new class of indole derivatives for use in treating allergy, asthma, rhinitis, dermatitis, B-cell lymphomas, tumors and diseases associated with bacterial, rhinovirus or respiratory syncytial virus (RSV) infections. It has now been found that the compounds of this invention are capable of modulating T helper (Th) cells, Thl/Th2, and thereby capable of inhibiting the transcription of interleukin-4 (IL-4) message, IL-4 release or IL-4 production.
    本发明公开了一类新的吲哚衍生物,用于治疗过敏、哮喘、鼻炎、皮炎、B 细胞淋巴瘤、肿瘤以及与细菌、鼻病毒或呼吸道合胞病毒(RSV)感染有关的疾病。现已发现,本发明的化合物能够调节 T 辅助(Th)细胞 Thl/Th2,从而能够抑制白细胞介素-4(IL-4)信息的转录、IL-4 的释放或 IL-4 的产生。
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