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1H-吲唑,3-[2-[4-(3-氯-2-甲基苯基)-1-哌嗪基]乙基]-1-(1H-咪唑-5-基甲基)-5,6-二甲氧基-,盐酸(1:2) | 162496-41-5

中文名称
1H-吲唑,3-[2-[4-(3-氯-2-甲基苯基)-1-哌嗪基]乙基]-1-(1H-咪唑-5-基甲基)-5,6-二甲氧基-,盐酸(1:2)
中文别名
——
英文名称
DY-9760E dihcl salt
英文别名
3-[2-[4-(3-chloro-2-methylphenyl)piperazin-1-yl]ethyl]-1-(1H-imidazol-5-ylmethyl)-5,6-dimethoxyindazole;dihydrochloride
1H-吲唑,3-[2-[4-(3-氯-2-甲基苯基)-1-哌嗪基]乙基]-1-(1H-咪唑-5-基甲基)-5,6-二甲氧基-,盐酸(1:2)化学式
CAS
162496-41-5
化学式
C26H33Cl3N6O2
mdl
——
分子量
567.9
InChiKey
IHRBZSIEWFFJQW-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

计算性质

  • 辛醇/水分配系数(LogP):
    5.0
  • 重原子数:
    37
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    71.4
  • 氢给体数:
    3
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    1-((5,6-dimethoxy-1-((1H-imidazol-4-yl)methyl)-1H-indazol-3-yl)ethyl)-4-(3-chloro-2-methylphenyl)piperazine 、 盐酸 为溶剂, 25.0 ℃ 、13.51 MPa 条件下, 反应 64.0h, 以to yield 5.5 g of the titled compound as a colorless prism的产率得到1H-吲唑,3-[2-[4-(3-氯-2-甲基苯基)-1-哌嗪基]乙基]-1-(1H-咪唑-5-基甲基)-5,6-二甲氧基-,盐酸(1:2)
    参考文献:
    名称:
    Piperazine derivatives
    摘要:
    化合物的化学式为(I):##STR1## 其中Q代表芳基,杂环基,二芳基甲基基团,由芳基和烷基组成的芳基烷基基团,烷基或环烷基,在其中,芳基,杂环基和二芳基甲基基团和芳基烷基基团的芳基部分可以被一个或多个取代基取代。R代表双环取代氮杂环基或取代苯基,其中氮杂环基由一个五元取代芳香或饱和环和一个六元环组成,其中含有一个或两个氮原子;Z代表烷基,烯基,含有羰基的烷基,含有羰基的烷基或草酰基,或其盐。该化合物具有钙调蛋白抑制活性,并可用作治疗循环器官或脑部区域疾病的治疗剂,这些疾病是由于钙调蛋白过度活化引起的。
    公开号:
    US05681954A1
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文献信息

  • Piperazine derivatives useful as calmodolin inhibitors
    申请人:DAIICHI PHARMACEUTICAL CO., LTD.
    公开号:EP0624584A1
    公开(公告)日:1994-11-17
    A compound represented by formula (I): wherein Q represents an aryl group, a heterocyclic group, a diarylmethyl group, an aralkyl group composed of an aryl group and an alkylene group, an alkyl group or a cycloalkyl group, in which the aryl group, heterocyclic group, and the aryl moiety of the diarylmethyl group and aralkyl group may be substituted with one or more substituents; R represents a bicyclic, substituted, nitrogen-containing heterocyclic group or a substituted phenyl group, in which the nitrogen-containing heterocyclic group is composed of a 5-membered, substituted, aromatic or saturated ring containing one or two nitrogen atoms and a 6-membered ring; and Z represents an alkylene group, an alkenylene group, an alkylene group, a carbonyl group, an alkylene group containing a carbonyl group or an oxalyl group, or a salt thereof. The compound has calmodulin inhibitory activity and is useful as a treating agent for diseases in the circulatory organs or in the cerebral region which are caused by excessive activation of calmodulin.
    式 (I) 所代表的化合物: 其中 Q 代表芳基、杂环基、二芳甲基、由芳基和亚烷基组成的芳烷基、烷基或环 烷基,其中芳基、杂环基以及二芳甲基和芳烷基的芳基可被一个或多个取代基取代;R 代表双环、取代的含氮杂环基团或取代的苯基,其中含氮杂环基团由含有一个或两个氮原子的五元环、取代的芳香环或饱和环以及六元环组成;以及 Z 代表烯基、烯基、亚烷基、羰基、含有羰基的亚烷基或草酰基、 或其盐。该化合物具有钙调蛋白抑制活性,可用于治疗因钙调蛋白过度活化而引起的循环器官或脑部疾病。
  • HYDRATE FOR MEDICINAL USE
    申请人:DAIICHI PHARMACEUTICAL CO., LTD.
    公开号:EP0792879A1
    公开(公告)日:1997-09-03
    Crystals of 3-[2-[4-(3-chloro-2-methylphenyl)-1-piperazinyl]ethyl]-5,6-dimethoxy-1-(4-imidazolylmethyl)-1H-indazole dihydrochloride which is a hydrate for pharmaceutical use having excellent characteristics as a pharmaceutical material that has high storage stability and which substantially has specified X-ray diffraction characteristics, more particularly, the dihydrochloride is 3.5-hydrate.
    3-[2-[4-(3-氯-2-甲基苯基)-1-哌嗪基]乙基]-5,6-二甲氧基-1-(4-咪唑基甲基)-1H-吲唑二盐酸盐的结晶,该结晶为药用水合物,具有作为药用材料的优异特性,储存稳定性高,且基本上具有规定的 X 射线衍射特性,更特别的是,该二盐酸盐为 3.5 水合物。
  • PIPERAZINE-CYCLODEXTRIN COMPLEXES
    申请人:DAIICHI PHARMACEUTICAL CO., LTD.
    公开号:EP1029872A1
    公开(公告)日:2000-08-23
    The present invention relates to a compound represented by formula (1): wherein Q, which may have a substituent, represents an aryl group, a heterocyclic group, a diarylmethyl group, or an aralkyl group; R, which may have a substituent, represents a bicyclic nitrogen-containing heterocyclic group or a phenyl group; and Z represents a C1-C3 alkylene group, a C2-C4 alkenylene group, a C1-C3 alkylene group having one hydroxyl group, a carbonyl moiety, a C1-C2 alkylene group containing one carbonyl moiety at one end or an intermediate position of the carbon chain, or an oxalyl group; or salts thereof and a piperazine-cyclodextrin complex combined with a water-soluble cyclodextrin derivative. The complex exhibits enhanced water solubility, excellent stability, and low topical stimulation and is useful as a therapeutic agent for circulatory diseases and diseases of the brain region.
    本发明涉及一种由式(1)表示的化合物: 其中 Q(可以有取代基)代表芳基、杂环基、二芳甲基或芳烷基;R(可以有取代基)代表双环含氮杂环基或苯基;Z 代表 C1-C3 亚烷基、C2-C4 烯基、具有一个羟基的 C1-C3 亚烷基、羰基、在碳链一端或中间位置含有一个羰基的 C1-C2 亚烷基或草酰基;或它们的盐以及与水溶性环糊精衍生物结合的哌嗪-环糊精复合物。 该复合物具有更强的水溶性、出色的稳定性和较低的局部刺激性,可用作循环系统疾病和脑部疾病的治疗剂。
  • Piperazine derivatives useful as calmodulin inhibitors
    申请人:DAIICHI PHARMACEUTICAL CO., LTD.
    公开号:EP0624584B1
    公开(公告)日:1998-08-19
  • EP0792879A4
    申请人:——
    公开号:EP0792879A4
    公开(公告)日:1998-02-25
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