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4-(1-(4-甲氧基苄基)-1H-吡唑-4-基)-2-(甲硫基)嘧啶 | 1020173-35-6

中文名称
4-(1-(4-甲氧基苄基)-1H-吡唑-4-基)-2-(甲硫基)嘧啶
中文别名
——
英文名称
4-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)-2-(methylthio)pyrimidine
英文别名
4-[1-[(4-methoxyphenyl)methyl]pyrazol-4-yl]-2-methylsulfanylpyrimidine
4-(1-(4-甲氧基苄基)-1H-吡唑-4-基)-2-(甲硫基)嘧啶化学式
CAS
1020173-35-6
化学式
C16H16N4OS
mdl
——
分子量
312.395
InChiKey
BCANXVLXOYGBMY-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):
    2.6
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    78.1
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-(1-(4-甲氧基苄基)-1H-吡唑-4-基)-2-(甲硫基)嘧啶5-氨基-4-氟-2-甲基苯酚间氯过氧苯甲酸potassium carbonate 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 2.0h, 以84%的产率得到5-(4-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrimidin-2-yloxy)-2-fluoro-4-methylbenzenamine
    参考文献:
    名称:
    [EN] CYCLOPROPANE AMIDES AND ANALOGS EXHIBITING ANTI-CANCER AND ANTI-PROLIFERATIVE ACTIVITIES
    [FR] AMIDES DE CYCLOPROPANE ET ANALOGUES PRÉSENTANT DES ACTIVITÉS ANTICANCÉREUSES ET ANTIPROLIFÉRATIVES
    摘要:
    本发明的化合物在治疗哺乳动物癌症,尤其是人类癌症方面具有实用性,包括但不限于恶性黑色素瘤、实体肿瘤、胶质母细胞瘤、卵巢癌、胰腺癌、前列腺癌、肺癌、乳腺癌、肾癌、肝癌、宫颈癌、原发肿瘤部位的转移、骨髓增生性疾病、慢性髓细胞白血病、白血病、乳头状甲状腺癌、非小细胞肺癌、间皮瘤、高嗜酸性综合征、胃肠道间质瘤、结肠癌、由高增殖导致失明的眼部疾病,包括各种视网膜病变、糖尿病视网膜病变、类风湿性关节炎、哮喘、慢性阻塞性肺病、肥大细胞增多症、肥大细胞白血病,以及由PDGFR-α激酶、PDGFR-β激酶、c-KIT激酶、cFMS激酶、c-MET激酶和致癌形式、异常融合蛋白和任何上述激酶的多态体引起的疾病。
    公开号:
    WO2010051373A1
  • 作为产物:
    描述:
    参考文献:
    名称:
    [EN] METHODS AND COMPOSITIONS FOR THE TREATMENT OF MYELOPROLIFERATIVE DISEASES AND OTHER PROLIFERATIVE DISEASES
    [FR] MÉTHODES ET COMPOSITIONS POUVANT ÊTRE UTILISÉES EN VUE DU TRAITEMENT DE MALADIES MYÉLOPROLIFÉRATIVES ET D'AUTRES MALADIES PROLIFÉRATIVES
    摘要:
    公开号:
    WO2013036232A3
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文献信息

  • KINASE INHIBITORS USEFUL FOR THE TREATMENT OF MYLEOPROLIFERATIVE DISEASES AND OTHER PROLIFERATIVE DISEASES
    申请人:Flynn L. Daniel
    公开号:US20080090856A1
    公开(公告)日:2008-04-17
    The present invention is concerned with novel compounds useful in the treatment of hyperproliferative diseases and mammalian cancers, especially human cancers. The invention also pertains to methods of modulating kinase activities, pharmaceutical compositions, and methods of treating individuals, incorporating or using the compounds. The preferred compounds are active small molecules set forth in formulae Ia-Iww.
    本发明涉及一种在治疗高增殖性疾病和哺乳动物癌症,尤其是人类癌症方面有用的新化合物。该发明还涉及调节激酶活性的方法、药物组合物以及治疗个体的方法,包括或使用这些化合物。优选的化合物是在公式Ia-Iww中列出的活性小分子。
  • CYCLOPROPANE AMIDES AND ANALOGS EXHIBITING ANTI-CANCER AND ANTI-PROLIFERATIVE ACTIVITIES
    申请人:Flynn Daniel L.
    公开号:US20100120806A1
    公开(公告)日:2010-05-13
    Compounds of the present invention find utility in the treatment of mammalian cancers and especially human cancers including, but not limited to, malignant melanomas, solid tumors, glioblastomas, ovarian cancer, pancreatic cancer, prostate cancer, lung cancers, breast cancers, kidney cancers, hepatic cancers, cervical carcinomas, metastasis of primary tumor sites, myeloproliferative diseases, chronic myelogenous leukemia, leukemias, papillary thyroid carcinoma, non-small cell lung cancer, mesothelioma, hypereosinophilic syndrome, gastrointestinal stromal tumors, colonic cancers, ocular diseases characterized by hyperproliferation leading to blindness including various retinopathies, diabetic retinopathy, rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, mastocytosis, mast cell leukemia, and diseases caused by PDGFR-α kinase, PDGFR-β kinase, c-KIT kinase, cFMS kinase, c-MET kinase, and oncogenic forms, aberrant fusion proteins and polymorphs of any of the foregoing kinases.
    本发明的化合物在哺乳动物癌症治疗中具有实用性,特别是人类癌症,包括但不限于恶性黑色素瘤、实体肿瘤、胶质母细胞瘤、卵巢癌、胰腺癌、前列腺癌、肺癌、乳腺癌、肾癌、肝癌、宫颈癌、原发肿瘤部位的转移、骨髓增生性疾病、慢性髓性白血病、白血病、乳头状甲状腺癌、非小细胞肺癌、间皮瘤、高嗜酸性综合症、胃肠道间质瘤、结肠癌、眼部疾病,其特征为细胞过度增殖导致失明,包括各种视网膜病变、糖尿病视网膜病变、类风湿性关节炎、哮喘、慢性阻塞性肺疾病、肥大细胞增多症、肥大细胞白血病以及由PDGFR-α激酶、PDGFR-β激酶、c-KIT激酶、cFMS激酶、c-MET激酶和任何上述激酶的癌变形式、异常融合蛋白和多态性引起的疾病。
  • N-acyl ureas exhibiting anti-cancer and anti-proliferative activities
    申请人:Deciphera Pharmaceuticals, LLC
    公开号:US08278331B2
    公开(公告)日:2012-10-02
    Compounds of the present invention find utility in the treatment of mammalian cancers and especially human cancers including, but not limited to, malignant melanomas, solid tumors, glioblastomas, ovarian cancer, pancreatic cancer, prostate cancer, lung cancers, breast cancers, kidney cancers, hepatic cancers, cervical carcinomas, metastasis of primary tumor sites, myeloproliferative diseases, chronic myelogenous leukemia, leukemias, papillary thyroid carcinoma, non-small cell lung cancer, mesothelioma, hypereosinophilic syndrome, gastrointestinal stromal tumors, colonic cancers, ocular diseases characterized by hyperproliferation leading to blindness including various retinopathies, diabetic retinopathy, rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, mastocytosis, mast cell leukemia, and diseases caused by PDGFR-α kinase, PDGFR-β kinase, c-KIT kinase, cFMS kinase, c-MET kinase, and oncogenic forms, aberrant fusion proteins and polymorphs of any of the foregoing kinases.
    本发明的化合物在哺乳动物癌症的治疗中具有实用性,特别是人类癌症,包括但不限于恶性黑色素瘤、实体肿瘤、胶质母细胞瘤、卵巢癌、胰腺癌、前列腺癌、肺癌、乳腺癌、肾癌、肝癌、宫颈癌、原发性肿瘤部位的转移、骨髓增生性疾病、慢性髓细胞白血病、白血病、乳头状甲状腺癌、非小细胞肺癌、间皮瘤、高嗜酸性综合征、胃肠间质肿瘤、结肠癌、眼部疾病,其特征为过度增殖导致失明,包括各种视网膜病变、糖尿病视网膜病变、类风湿性关节炎、哮喘、慢性阻塞性肺疾病、肥大细胞增多症、肥大细胞白血病,以及由PDGFR-α激酶、PDGFR-β激酶、c-KIT激酶、cFMS激酶、c-MET激酶和任何上述激酶的癌变形式、异常融合蛋白和多态性引起的疾病。
  • Kinase inhibitors useful for the treatment of myleoproliferative diseases and other proliferative diseases
    申请人:Deciphera Pharmaceuticals, LLC
    公开号:US07790756B2
    公开(公告)日:2010-09-07
    The present invention is concerned with novel compounds useful in the treatment of hyperproliferative diseases and mammalian cancers, especially human cancers. The invention also pertains to methods of modulating kinase activities, pharmaceutical compositions, and methods of treating individuals, incorporating or using the compounds. The preferred compounds are active small molecules set forth in formulae Ia-Iww.
    本发明涉及一种在治疗增生性疾病和哺乳动物癌症,特别是人类癌症方面有用的新型化合物。该发明还涉及调节激酶活性的方法、制药组合物以及使用该化合物治疗个体的方法。首选的化合物是公式Ia-Iww中列出的活性小分子。
  • Kinase Inhibitors Useful for the Treatment of Myleoproliferative Diseases and other Proliferative Diseases
    申请人:Flynn Daniel L.
    公开号:US20110136760A1
    公开(公告)日:2011-06-09
    The present invention is concerned with novel compounds useful in the treatment of hyperproliferative diseases and mammalian cancers, especially human cancers. The invention also pertains to methods of modulating kinase activities, pharmaceutical compositions, and methods of treating individuals, incorporating or using the compounds. The preferred compounds are active small molecules set forth in formulae Ia-Iww.
    本发明涉及一种新型化合物,可用于治疗过度增殖性疾病和哺乳动物癌症,特别是人类癌症。本发明还涉及调节激酶活性的方法、制药组合物以及治疗个体的方法,包括或使用该化合物。优选的化合物是在公式Ia-Iww中列出的活性小分子。
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