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2,4-dichloro-5-trifluoromethylsulphanyl-pyrimidine | 108222-71-5

中文名称
——
中文别名
——
英文名称
2,4-dichloro-5-trifluoromethylsulphanyl-pyrimidine
英文别名
2,4-dichloro-5-(trifluoromethylsulfanyl)pyrimidine
2,4-dichloro-5-trifluoromethylsulphanyl-pyrimidine化学式
CAS
108222-71-5
化学式
C5HCl2F3N2S
mdl
MFCD28040367
分子量
249.044
InChiKey
UCQPIXYDODRKCJ-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:
    195.3±40.0 °C(Predicted)
  • 密度:
    1.72±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.8
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    51.1
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    2,4-dichloro-5-trifluoromethylsulphanyl-pyrimidineantimony(III) trioxide 、 potassium fluoride 作用下, 反应 2.0h, 以63%的产率得到5-Trifluormethylmercapto-2,4-difluor-pyrimidin
    参考文献:
    名称:
    Haas, A.; Lieb, M., Journal of Heterocyclic Chemistry, 1986, vol. 23, p. 1079 - 1084
    摘要:
    DOI:
  • 作为产物:
    描述:
    5-trifluoromethylmercapto uracil 在 三氯氧磷 作用下, 反应 4.0h, 以45.4%的产率得到2,4-dichloro-5-trifluoromethylsulphanyl-pyrimidine
    参考文献:
    名称:
    Haas, A.; Lieb, M., Journal of Heterocyclic Chemistry, 1986, vol. 23, p. 1079 - 1084
    摘要:
    DOI:
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文献信息

  • Pyrimidine derivatives
    申请人:Boehringer Ingelheim Pharma KG
    公开号:US20030171359A1
    公开(公告)日:2003-09-11
    The present invention relates to trisubstituted pyrimidines of formula (I) 1 wherein 0R a to R e are defined as in claim 1, which are suitable for the treatment of illnesses characterised by excessive or abnormal cell proliferation, the use thereof for preparing a pharmaceutical composition with the abovementioned properties, and processes for the preparation thereof.
    本发明涉及式(I)的三取代嘧啶化合物,其中R至R如权利要求书中所定义,适用于治疗由细胞过度或异常增殖特征的疾病,其用于制备具有上述特性的药物组合物,以及其制备方法。
  • PYRIMIDINE DERIVATIVES
    申请人:DAHMANN Georg
    公开号:US20100152167A1
    公开(公告)日:2010-06-17
    The present invention relates to trisubstituted pyrimidines of formula (I) wherein 0R a to R e are defined as in claim 1 , which are suitable for the treatment of illnesses characterised by excessive or abnormal cell proliferation, the use thereof for preparing a pharmaceutical composition with the abovementioned properties, and processes for the preparation thereof.
    本发明涉及式(I)的三取代嘧啶,其中0R至Re如权利要求1中所定义,适用于治疗由过度或异常细胞增殖所表征的疾病,其用于制备具有上述特性的药物组合物,以及其制备过程。
  • [EN] INHIBITORS OF CYCLIN‑DEPENDENT KINASE 12 (CDK12)<br/>[FR] INHIBITEURS DE LA KINASE 12 DÉPENDANTE DE LA CYCLINE (CDK12)
    申请人:SYROS PHARMACEUTICALS INC
    公开号:WO2023091726A1
    公开(公告)日:2023-05-25
    The present invention provides chemical compounds that inhibit one or more families of kinases (e.g., serine/threonine kinases, including one or more of the families of CDK proteins, and in particular, CDK12). More specifically, the present invention provides CDK12 inhibitors, of formula (I), pharmaceutically acceptable salts and isotopically labeled derivatives thereof, pharmaceutical compositions containing the compounds/inhibitors, and methods of their synthesis and use in treating proliferative diseases (e.g., a bladder cancer, a breast cancer, Ewing's sarcoma, a gastric cancer, a gastrointestinal cancer, a hematologic cancer, a lung cancer (e.g., small cell lung cancer (SCLC)), an ovarian cancer (e.g., a high grade serous ovarian cancer), a pancreatic cancer (e.g., pancreatic ductal adenocarcinoma (PDAC)), a brain cancer (e.g., glioblastoma), or a prostate cancer), alone or in combination with a second therapeutic agent. The proliferative disease can be a cancer, benign neoplasm, or pathologic angiogenesis, and any of the therapeutic methods or uses described herein can include a step of diagnosing the patient's disease. In other embodiments of the invention, the compositions described herein (e.g., the compounds, pharmaceutical compositions, and kits containing them) are used for the treatment of myotonic dystrophy (type 1 or type 2).
    本发明提供了抑制一个或多个激酶家族(如丝氨酸/苏氨酸激酶,包括一个或多个CDK蛋白家族,特别是CDK12)的化合物。更具体地说,本发明提供了式 (I) 的 CDK12 抑制剂、其药学上可接受的盐和同位素标记的衍生物、含有该化合物/抑制剂的药物组合物,以及它们的合成方法和用于治疗增殖性疾病(如、膀胱癌、乳腺癌、尤文氏肉瘤、胃癌、胃肠道癌、血癌、肺癌(如小细胞肺癌 (SCLC))、卵巢癌(如、胰腺癌(如胰腺导管腺癌 (PDAC))、脑癌(如胶质母细胞瘤)或前列腺癌)。增殖性疾病可以是癌症、良性肿瘤或病理性血管生成,本文所述的任何治疗方法或用途都可以包括诊断患者疾病的步骤。在本发明的其他实施方案中,本文所述的组合物(如化合物、药物组合物和含有它们的试剂盒)用于治疗肌营养不良症(1 型或 2 型)。
  • PYRIMIDINDERIVATE, ARZNEIMITTEL ENTHALTEND DIESE VERBINDUNGEN, DEREN VERWENDUNG UND VERFAHREN ZU IHRER HERSTELLUNG
    申请人:Boehringer Ingelheim Pharma GmbH & Co.KG
    公开号:EP1438053A1
    公开(公告)日:2004-07-21
  • Pyrimidinderivate, Arzneimittel enthaltend diese Verbindungen, deren Verwendung und Verfahren zu ihrer Herstellung
    申请人:Boehringer Ingelheim Pharma GmbH & Co. KG
    公开号:EP2090571B1
    公开(公告)日:2012-05-16
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