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8-溴-2-氟-1,5-二氮杂萘 | 1432322-85-4

中文名称
8-溴-2-氟-1,5-二氮杂萘
中文别名
——
英文名称
8-bromo-2-fluoro-1,5-naphthyridine
英文别名
——
8-溴-2-氟-1,5-二氮杂萘化学式
CAS
1432322-85-4
化学式
C8H4BrFN2
mdl
MFCD24539414
分子量
227.036
InChiKey
LYJLCBJPUTZONT-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:
    318.3±37.0 °C(Predicted)
  • 密度:
    1.741±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • 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:
    3

安全信息

  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

反应信息

  • 作为反应物:
    描述:
    8-溴-2-氟-1,5-二氮杂萘N-碘代丁二酰亚胺四(三苯基膦)钯sodium carbonate 、 Ephos Pd G4caesium carbonate 作用下, 以 1,4-二氧六环N,N-二甲基甲酰胺叔丁醇 为溶剂, 反应 3.0h, 生成 2-[6-(dimethylamino)-1,5-naphthyridin-4-yl]-3-[(3-fluoro-2-methoxyphenyl)amino]-1H,5H,6H,7H-pyrrolo[3,2-c]pyridin-4-one
    参考文献:
    名称:
    [EN] HETEROCYCLIC INHIBITORS OF EGFR AND/OR HER2, FOR USE IN THE TREATMENT OF CANCER
    [FR] MÉTHODES DE TRAITEMENT DU CANCER
    摘要:
    公开号:
    WO2022076831A3
  • 作为产物:
    描述:
    2-氟-5-氨基吡啶乙醇三溴化磷 作用下, 以 二苯醚联苯N,N-二甲基甲酰胺 为溶剂, 反应 3.58h, 生成 8-溴-2-氟-1,5-二氮杂萘
    参考文献:
    名称:
    [EN] USE OF MACROCYCLIC COMPOUNDS IN METHODS OF TREATING CANCER
    [FR] UTILISATION DE COMPOSÉS MACROCYCLIQUES DANS DES MÉTHODES DE TRAITEMENT DE CANCER
    摘要:
    本公开提供化合物(例如,化合物或药物可接受的盐,和/或水合物,和/或共晶体,和/或化合物的药物组合物),其抑制表皮生长因子受体(EGFR,ERBB1)和/或人类表皮生长因子受体2(HER2,ERBB2)。这些化合物是有用的,例如,用于治疗某种情况,疾病或障碍,在该情况,疾病或障碍中增加(例如过度)的EGFR和/或HER2激活对该情况,疾病或障碍的病理生理和/或症状和/或进展有贡献的受试者(例如,人类)。本公开还提供包含相同物质的组合物以及使用和制备相同物质的方法。
    公开号:
    WO2022098992A1
点击查看最新优质反应信息

文献信息

  • [EN] CASEIN KINASE 1 DELTA MODULATORS<br/>[FR] MODULATEURS DE LA CASÉINE KINASE 1 DELTA
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2022058921A1
    公开(公告)日:2022-03-24
    A compound of Formula (I) or Formula (II), pharmaceutical compositions containing them, methods of making them, and methods of using them including methods for treating disease states, disorders, and conditions associated with casein kinase 1 delta (CSNK1D) modulation, such as those associated with mood/psychiatric disorders, neurodegenerative diseases, cancers, addiction and substance abuse disorders, pain, and metabolic diseases.or Wherein R1, R2, R3, R4, R1a, R2a, R3, and R4aare defined herein.
    公式(I)或公式(II)的化合物,含有它们的药物组合物,制备它们的方法以及使用它们的方法,包括用于治疗与酪蛋白激酶1δ(CSNK1D)调节相关的疾病状态、紊乱和情况的方法,例如与情绪/精神紊乱、神经退行性疾病、癌症、成瘾和物质滥用紊乱、疼痛和代谢性疾病相关的方法。其中R1、R2、R3、R4、R1a、R2a、R3和R4a在此定义。
  • One-step hydroxylation of aryl and heteroaryl fluorides using mechanochemistry
    作者:Eduardo Rodrigo、Rainer Wiechert、Magnus W. Walter、Wilfried Braje、Hervé Geneste
    DOI:10.1039/d1gc04361g
    日期:——
    Simple use of KOH allows the direct F to OH exchange of aromatic and heteroaromatic substrates under mechanochemical conditions. The reaction is performed in the absence of solvent with potassium hydroxide as OH source. As a result, this approach is both more atom economical and environmentally friendly than previously described methods for this transformation.
    简单地使用 KOH 可以在机械化学条件下实现芳族和杂芳族底物的直接 F 到 OH 交换。该反应在没有溶剂的情况下以氢氧化钾作为OH源进行。因此,这种方法比之前描述的这种转化方法更原子经济和环境友好。
  • [EN] BICYCLIC COMPOUNDS FOR USE IN THE TREATMENT CANCER<br/>[FR] COMPOSÉS BICYCLIQUES DESTINÉS À ÊTRE UTILISÉS DANS LE TRAITEMENT DU CANCER
    申请人:SCORPION THERAPEUTICS INC
    公开号:WO2022072634A1
    公开(公告)日:2022-04-07
    This disclosure provides chemical entities (e.g., a compound or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that inhibit epidermal growth factor receptor (EGFR, ERBB1) and/or Human epidermal growth factor receptor 2 (HER2, ERBB2). These chemical entities are useful, e.g., for treating a condition, disease or disorder in which increased (e.g., excessive) EGFR and/or HER2 activation contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human). This disclosure also provides compositions containing the same as well as methods of using and making the same.
    本公开提供化学实体(例如,化合物或药学上可接受的盐,和/或合物,和/或共晶体,和/或药物组合物),其抑制表皮生长因子受体(EGFR,ERBB1)和/或人类表皮生长因子受体2(HER2,ERBB2)。这些化学实体是有用的,例如,用于治疗某种疾病或疾病,其中增加(例如,过度)EGFR和/或HER2激活有助于病理和/或症状和/或疾病或疾病的进展(例如,癌症)在受试者(例如,人类)中。本公开还提供包含相同化学实体的组合物以及使用和制备相同的方法。
  • [EN] BICYCLIC DERIVATIVES WHICH CAN BE USED TO TREAT CANCER<br/>[FR] DÉRIVÉS BICYCLIQUES POUVANT ÊTRE UTILISÉS POUR TRAITER LE CANCER
    申请人:SCORPION THERAPEUTICS INC
    公开号:WO2022197913A1
    公开(公告)日:2022-09-22
    This disclosure provides chemical entities (e.g., a compound or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that inhibit epidermal growth factor receptor (EGFR, ERBB1) and/or Human epidermal growth factor receptor 2 (HER2, ERBB2). These chemical entities are useful, e.g., for treating a condition, disease or disorder in which increased (e.g., excessive) EGFR and/or HER2 activation contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human). This disclosure also provides compositions containing the same as well as methods of using and making the same.
    本公开提供化学实体(例如化合物或药物可接受的盐,和/或合物,和/或共晶体,和/或化合物的药物组合物),其抑制表皮生长因子受体(EGFR,ERBB1)和/或人类表皮生长因子受体2(HER2,ERBB2)的作用。这些化学实体是有用的,例如,用于治疗在其中增加(例如过度)EGFR和/或HER2激活导致病理学和/或症状和/或疾病或障碍(例如癌症)的情况,疾病或障碍的主体(例如人类)。本公开还提供包含相同的组合物以及使用和制造相同的方法。
  • [EN] METHODS FOR TREATING CANCER<br/>[FR] MÉTHODES DE TRAITEMENT DU CANCER
    申请人:[en]SCORPION THERAPEUTICS, INC.
    公开号:WO2022076831A2
    公开(公告)日:2022-04-14
    This disclosure provides chemical entities (e.g., a compound or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that inhibit epidermal growth factor receptor (EGFR, ERBB1) and/or Human epidermal growth factor receptor 2 (HER2, ERBB2). These chemical entities are useful, e.g., for treating a condition, disease or disorder in which increased (e.g., excessive) EGFR and/or HER2 activation contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human). This disclosure also provides compositions containing the same as well as methods of using and making the same.
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