摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-(2-噻吩甲基)-1H-吡唑-5-胺 | 4394-26-7

中文名称
1-(2-噻吩甲基)-1H-吡唑-5-胺
中文别名
——
英文名称
1-(α-Thienylmethyl)-5-aminopyrazol
英文别名
2-thiophen-2-ylmethyl-2H-pyrazol-3-ylamine;1-(Thiophen-2-ylmethyl)-1H-pyrazol-5-amine;2-(thiophen-2-ylmethyl)pyrazol-3-amine
1-(2-噻吩甲基)-1H-吡唑-5-胺化学式
CAS
4394-26-7
化学式
C8H9N3S
mdl
MFCD06358647
分子量
179.246
InChiKey
KFEVMOCBDLBBKX-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:
    72-73 °C
  • 沸点:
    380.7±27.0 °C(Predicted)
  • 密度:
    1.36±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.125
  • 拓扑面积:
    72.1
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2934999090

反应信息

  • 作为产物:
    描述:
    3-[2-(thiophen-2-ylmethylidene)hydrazinyl]propanenitrile 在 sodium 作用下, 以 正丁醇 为溶剂, 生成 1-(2-噻吩甲基)-1H-吡唑-5-胺
    参考文献:
    名称:
    Approach to the Library of Fused Pyridine-4-carboxylic Acids by Combes-Type Reaction of Acyl Pyruvates and Electron-Rich Amino Heterocycles
    摘要:
    A library of fused pyridine-4-carboxylic acids (including pyrazolo[3,4-b]pyridines, isoxazolo[5,4-b]pyridines, furo[2,3-b]pyridines, thieno[2,3-b]pyridines, and pyrido[2,3-d]pyrimidines) was generated by Combes-type reaction of acyl pyruvates and electron-rich amino heterocycles followed by hydrolysis of the ester. The library members were also demonstrated to undergo the standard combinatorial transformations including amide coupling and esterification, as well as less common heterocyclizations to 1,2,4-triazoles and 1,2,4-oxadiazoles.
    DOI:
    10.1021/cc100040q
点击查看最新优质反应信息

文献信息

  • [EN] MULTISUBSTITUTED AROMATIC COMPOUNDS AS SERINE PROTEASE INHIBITORS<br/>[FR] COMPOSÉS AROMATIQUES MULTISUBSTITUÉS EN TANT QU'INHIBITEURS DE SÉRINE PROTÉASE
    申请人:VERSEON INC
    公开号:WO2014145986A1
    公开(公告)日:2014-09-18
    There are provided inter alia multisubstituted aromatic compounds useful for the inhibition of kallikrein, which compounds include substituted pyrazolyl or substituted triazolyl. There are additionally provided pharmaceutical compositions. There are additionally provided methods of treating and preventing certain diseases or disorders, which disease or disorder is amenable to treatment or prevention by the inhibition of kallikrein.
    提供了用于抑制激肽酶的多取代芳香化合物,其中这些化合物包括取代吡唑基或取代三唑基。此外还提供了药物组合物。此外还提供了治疗和预防某些疾病或疾病的方法,这些疾病或疾病可通过抑制激肽酶来治疗或预防。
  • MULTISUBSTITUTED AROMATIC COMPOUNDS AS INHIBITORS OF THROMBIN
    申请人:VERSEON CORPORATION
    公开号:US20170326125A1
    公开(公告)日:2017-11-16
    There are provided inter alia multisubstituted aromatic compounds useful for the inhibition of thrombin, which compounds include substituted pyrazolyl or substituted triazolyl. There are additionally provided pharmaceutical compositions. There are additionally provided methods of treating and preventing a disease or disorder, which disease or disorder is amenable to treatment or prevention by the inhibition of thrombin.
    提供了用于抑制凝血酶的多取代芳香化合物,其中化合物包括取代的吡唑基或取代的三唑基。此外还提供了药物组合物。此外还提供了治疗和预防疾病或紊乱的方法,该疾病或紊乱可通过抑制凝血酶进行治疗或预防。
  • TETRAZOLE COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS
    申请人:Aissaoui Hamed
    公开号:US20110086889A1
    公开(公告)日:2011-04-14
    The invention relates to tetrazole compounds of formula (I) wherein X, Y, Z, R 1 , R 2 and R 3 are as described in the description; to pharmaceutically acceptable salts thereof, and to the use of such compounds use as medicaments, especially as orexin receptor antagonists.
    该发明涉及式(I)的四唑化合物,其中X、Y、Z、R1、R2和R3如描述中所述;其药学上可接受的盐,以及将这些化合物用作药物,特别是促进睡眠的药物。
  • MULTISUBSTITUTED AROMATIC COMPOUNDS AS SERINE PROTEASE INHIBITORS
    申请人:VERSEON CORPORATION
    公开号:US20160024047A1
    公开(公告)日:2016-01-28
    There are provided inter alia multisubstituted aromatic compounds useful for the inhibition of kallikrein, which compounds include substituted pyrazolyl or substituted triazolyl. There are additionally provided pharmaceutical compositions. There are additionally provided methods of treating and preventing certain diseases or disorders, which disease or disorder is amenable to treatment or prevention by the inhibition of kallikrein.
    本发明提供了多取代芳香化合物,其中包括取代的吡唑基或取代的三唑基,用于抑制卡利肽酶,另外还提供了制药组合物。本发明还提供了治疗和预防某些疾病或疾病的方法,该疾病或疾病可通过抑制卡利肽酶来治疗或预防。
  • Multisubstituted aromatic compounds as serine protease inhibitors
    申请人:VERSEON CORPORATION
    公开号:US10058541B2
    公开(公告)日:2018-08-28
    There are provided inter alia multisubstituted aromatic compounds useful for the inhibition of kallikrein, which compounds include substituted pyrazolyl or substituted triazolyl. There are additionally provided pharmaceutical compositions. There are additionally provided methods of treating and preventing certain diseases or disorders, which disease or disorder is amenable to treatment or prevention by the inhibition of kallikrein.
    除其他外,还提供了可用于抑制卡利克林的多取代芳香族化合物,这些化合物包括取代的吡唑基或取代的三唑基。另外还提供了药物组合物。此外,还提供了治疗和预防某些疾病或失调的方法,这些疾病或失调可通过抑制卡利克林来治疗或预防。
查看更多

同类化合物

伊莫拉明 (5aS,6R,9S,9aR)-5a,6,7,8,9,9a-六氢-6,11,11-三甲基-2-(2,3,4,5,6-五氟苯基)-6,9-甲基-4H-[1,2,4]三唑[3,4-c][1,4]苯并恶嗪四氟硼酸酯 (5-氨基-1,3,4-噻二唑-2-基)甲醇 齐墩果-2,12-二烯[2,3-d]异恶唑-28-酸 黄曲霉毒素H1 高效液相卡套柱 非昔硝唑 非布索坦杂质Z19 非布索坦杂质T 非布索坦杂质K 非布索坦杂质E 非布索坦杂质67 非布索坦杂质65 非布索坦杂质64 非布索坦杂质61 非布索坦代谢物67M-4 非布索坦代谢物67M-2 非布索坦代谢物 67M-1 非布索坦-D9 非布索坦 非唑拉明 雷西纳德杂质H 雷西纳德 阿西司特 阿莫奈韦 阿米苯唑 阿米特罗13C2,15N2 阿瑞匹坦杂质 阿格列扎 阿扎司特 阿尔吡登 阿塔鲁伦中间体 阿培利司N-1 阿哌沙班杂质26 阿哌沙班杂质15 阿可替尼 阿作莫兰 阿佐塞米 镁(2+)(Z)-4'-羟基-3'-甲氧基肉桂酸酯 锌1,2-二甲基咪唑二氯化物 铵2-(4-氯苯基)苯并恶唑-5-丙酸盐 铬酸钠[-氯-3-[(5-二氢-3-甲基-5-氧代-1-苯基-1H-吡唑-4-基)偶氮]-2-羟基苯磺酸基][4-[(3,5-二氯-2-羟基苯 铁(2+)乙二酸酯-3-甲氧基苯胺(1:1:2) 钠5-苯基-4,5-二氢吡唑-1-羧酸酯 钠3-[2-(2-壬基-4,5-二氢-1H-咪唑-1-基)乙氧基]丙酸酯 钠3-(2H-苯并三唑-2-基)-5-仲-丁基-4-羟基苯磺酸酯 钠(2R,4aR,6R,7R,7aS)-6-(2-溴-9-氧代-6-苯基-4,9-二氢-3H-咪唑并[1,2-a]嘌呤-3-基)-7-羟基四氢-4H-呋喃并[3,2-D][1,3,2]二氧杂环己膦烷e-2-硫醇2-氧化物 野麦枯 野燕枯 醋甲唑胺