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4-chloro-2-vinylpyrimidine | 1378818-05-3

中文名称
——
中文别名
——
英文名称
4-chloro-2-vinylpyrimidine
英文别名
4-chloro-2-ethenylpyrimidine
4-chloro-2-vinylpyrimidine化学式
CAS
1378818-05-3
化学式
C6H5ClN2
mdl
——
分子量
140.572
InChiKey
FNWCYMQLBUDFMP-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):
    2
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    25.8
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    重氮乙酸乙酯4-chloro-2-vinylpyrimidine甲苯 为溶剂, 以21 %的产率得到rac-ethyl (1S*,2S*)-2-(4-chloropyrimidin-2-yl)cyclopropane-1-carboxylate
    参考文献:
    名称:
    [EN] HETEROARYL INHIBITORS OF PLASMA KALLIKREIN
    [FR] INHIBITEURS HÉTÉROARYLE DE LA KALLICRÉINE PLASMATIQUE
    摘要:
    本发明提供了一种化合物及其组合物,可用作血浆卡利肌酶的抑制剂,并表现出相同的理想特性。
    公开号:
    WO2022197758A1
  • 作为产物:
    描述:
    参考文献:
    名称:
    [EN] COMPOUNDS FOR THE TREATMENT OF PARAMOXYVIRUS VIRAL INFECTIONS
    [FR] COMPOSÉS POUR LE TRAITEMENT D'INFECTIONS VIRALES PAR PARAMYXOVIRUS
    摘要:
    本文披露了新的抗病毒化合物,以及包含一种或多种抗病毒化合物的药物组合物,并且揭示了合成这些化合物的方法。本文还披露了利用一种或多种小分子化合物改善和/或治疗副黏病毒病毒感染的方法。副黏病毒感染的例子包括由人类呼吸道合胞病毒(RSV)引起的感染。
    公开号:
    WO2014031784A1
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文献信息

  • [EN] 4-HETEROARYLMETHYL SUBSTITUTED PHTHALAZINONE DERIVATIVES<br/>[FR] DERIVES DE PHTALAZINONE SUBSTITUES PAR UN GROUPE 4-HETEROARYLMETHYLE
    申请人:KUDOS PHARM LTD
    公开号:WO2006021801A1
    公开(公告)日:2006-03-02
    A compound of formula (I): for use in treating cancer or other diseases ameliorated by the inhibition of PARP, wherein: A and B together represent an optionally substituted, fused aromatic ring; X can be NRx or CRxRy; if X=NRx then n is 1 or 2 and if X=CRxRy then n is 1; Rx is selected from the group consisting of H, optionally substituted C1-20 alkyl, C5-20 aryl, C3-20 heterocyclyl, amido, thioamido, ester, acyl, and sulfonyl groups; Ry is selected from H, hydroxy, amino; or Rx and Ry may together form a spiro-C3-7 cycloalkyl or heterocyclyl group; RC1 and RC2 are independently selected from the group consisting of hydrogen and C1-4 alkyl, or when X is CRxRy, RC1, RC2, Rx and Ry, together with the carbon atoms to which they are attached, may form an optionally substituted fused aromatic ring; R1 is selected from H and halo; and Het is selected from: (i) formula (i), where Y1 is selected from CH and N, Y2 is selected from CH and N, Y3 is selected from CH, CF and N, where only one or two of Y1, Y2 and Y3 can be N; and (ii) formula (ii), where Q is O or S.
    化合物的公式(I):用于治疗癌症或其他通过抑制PARP改善的疾病,其中:A和B一起代表可选择取代的融合芳香环;X可以是NRx或CRxRy;如果X=NRx,则n为1或2,如果X=CRxRy,则n为1;Rx从H,可选择取代的C1-20烷基,C5-20芳基,C3-20杂环烷基,酰胺,酰胺,酯,酰基和磺酰基组中选择;Ry从H,羟基,基中选择;或Rx和Ry可以一起形成螺环C3-7环烷基或杂环烷基;RC1和RC2独立地从氢和C1-4烷基组中选择,或者当X为CRxRy时,RC1、RC2、Rx和Ry,连同它们附着的碳原子,可以形成可选择取代的融合芳香环;R1从H和卤素中选择;Het从以下中选择:(i)公式(i),其中Y1从CH和N中选择,Y2从CH和N中选择,Y3从CH,CF和N中选择,其中只有一个或两个Y1、Y2和Y3可以是N;和(ii)公式(ii),其中Q为O或S。
  • COMPOUNDS FOR THE TREATMENT OF PARAMOXYVIRUS VIRAL INFECTIONS
    申请人:Alios Bio Pharma, Inc.
    公开号:US20150238498A1
    公开(公告)日:2015-08-27
    Disclosed herein are new antiviral compounds, together with pharmaceutical compositions that include one or more antiviral compounds, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a paramyxovirus viral infection with one or more small molecule compounds. Examples of paramyxovirus infection include an infection caused by human respiratory syncytial virus (RSV).
    本文披露了一些新的抗病毒化合物,以及包含一种或多种抗病毒化合物的药物组合物和合成它们的方法。还披露了使用一种或多种小分子化合物改善和/或治疗副黏液病毒病毒感染的方法。副黏液病毒感染的例子包括由人类呼吸道合胞病毒(RSV)引起的感染。
  • PHTHALAZINONE DERIVATIVES
    申请人:Javaid Muhammad Hashim
    公开号:US20090163477A1
    公开(公告)日:2009-06-25
    A compound of formula (I): for use in treating cancer or other diseases ameliorated by the inhibition of PARP, wherein: A and B together represent an optionally substituted, fused aromatic ring; X can be NR X or CR X R Y ; if X═NR X then n is 1 or 2 and if X═CR X R Y then n is 1; R X is selected from the group consisting of H, optionally substituted C 1-20 alkyl, C 5-20 aryl, C 3-20 heterocyclyl, amido, thioamido, ester, acyl, and sulfonyl groups; R Y is selected from H, hydroxy, amino; or R X and R Y may together form a spiro-C 3-7 cycloalkyl or heterocyclyl group; R C1 and R C2 are independently selected from the group consisting of hydrogen and C 1-4 alkyl, or when X is CR X R Y , R C1 , R C1 , R C2 , R X and R Y , together with the carbon atoms to which they are attached, may form an optionally substituted fused aromatic ring; R 1 is selected from H and halo; and Het is selected from: where Y 1 is selected from CH and N, Y 2 is selected from CH and N, Y 3 is selected from CH, CF and N, where only one or two of Y 1 , Y 2 and Y 3 can be N; and where Q is O or S.
    公式(I)的化合物:用于治疗由于PARP抑制而改善的癌症或其他疾病,其中:A和B共同表示一个可选取的,融合芳香环;X可以是NRX或CRXRY;如果X═NRX,则n为1或2,如果X═CRXRY,则n为1;RX从H,可选取的取代C1-20烷基,C5-20芳基,C3-20杂环基,酰胺,酰胺,酯,酰基和磺酰基组中选择;RY从H,羟基,基中选择;或者RX和RY可以共同形成一个螺旋C3-7环烷基或杂环基;RC1和RC2从氢和C1-4烷基中独立选择,或者当X为CRXRY时,RC1,RC1,RC2,RX和RY可以与它们附着的碳原子共同形成一个可选取的融合芳香环;R1从H和卤素中选择;Het从以下中选择:其中Y1从CH和N中选择,Y2从CH和N中选择,Y3从CH,CF和N中选择,其中只有一个或两个Y1,Y2和Y3可以是N;并且Q为O或S。
  • Compounds for the treatment of paramyxovirus viral infections
    申请人:JANSSEN BIOPHARMA, INC.
    公开号:US11014935B2
    公开(公告)日:2021-05-25
    Disclosed herein are new antiviral compounds, together with pharmaceutical compositions that include one or more antiviral compounds, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a paramyxovirus viral infection with one or more small molecule compounds. Examples of paramyxovirus infection include an infection caused by human respiratory syncytial virus (RSV).
    本文公开了新的抗病毒化合物,以及包括一种或多种抗病毒化合物的药物组合物和合成这些化合物的方法。本文还公开了用一种或多种小分子化合物改善和/或治疗副黏液病毒感染的方法。副粘病毒感染的例子包括由人类呼吸道合胞病毒(RSV)引起的感染。
  • SUBSTITUTED NITROGEN CONTAINING COMPOUNDS
    申请人:Bristol-Myers Squibb Company
    公开号:EP3630752B1
    公开(公告)日:2021-06-30
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