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2-chloro-N-(6-methoxypyridin-3-yl)quinazolin-4-amine | 827030-59-1

中文名称
——
中文别名
——
英文名称
2-chloro-N-(6-methoxypyridin-3-yl)quinazolin-4-amine
英文别名
(2-chloro-quinazolin-4-yl)-(6-methoxy-pyridin-3-yl)-amine
2-chloro-N-(6-methoxypyridin-3-yl)quinazolin-4-amine化学式
CAS
827030-59-1
化学式
C14H11ClN4O
mdl
——
分子量
286.721
InChiKey
NFPIHMWCQJLBBI-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):
    3.6
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    59.9
  • 氢给体数:
    1
  • 氢受体数:
    5

SDS

SDS:8fa69494163c169a5f54d25da300d5e1
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上下游信息

  • 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:
    2-chloro-N-(6-methoxypyridin-3-yl)quinazolin-4-amine碘甲烷 在 sodium hydride 作用下, 以 DMF (N,N-dimethyl-formamide) 为溶剂, 反应 2.0h, 以70%的产率得到2-chloro-N-(6-methoxypyridin-3-yl)-N-methylquinazolin-4-amine
    参考文献:
    名称:
    [EN] 4-ARYLAMINO-QUINAZOLINES AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS
    [FR] COMPOSES ET LEUR UTILISATION THERAPEUTIQUE
    摘要:
    公开号:
    WO2005003100A3
  • 作为产物:
    描述:
    5-氨基-2-甲氧基吡啶2,4-二氯喹唑啉sodium acetate 作用下, 以 四氢呋喃 为溶剂, 反应 0.75h, 以98%的产率得到2-chloro-N-(6-methoxypyridin-3-yl)quinazolin-4-amine
    参考文献:
    名称:
    [EN] 4-ARYLAMINO-QUINAZOLINES AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS
    [FR] COMPOSES ET LEUR UTILISATION THERAPEUTIQUE
    摘要:
    公开号:
    WO2005003100A3
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文献信息

  • [EN] COMPOUNDS FOR USE IN INHIBITING HIV CAPSID ASSEMBLY<br/>[FR] COMPOSÉS POUR UTILISATION DANS L'INHIBITION DE L'ASSEMBLAGE DE CAPSIDE DE VIH
    申请人:RUPRECHT KARLS UNIVERSITÄT HEIDELBERG
    公开号:WO2014128206A1
    公开(公告)日:2014-08-28
    The present invention relates to a compound or a pharmaceutically acceptable salt or solvate thereof for use in inhibiting HIV capsid assembly, the compound comprising the core structure wherein E is CR7or S, and wherein f is 0 or 1, and wherein in case E is S, f is 0, and wherein the core structure is at least substituted in 2 and 4 position, and wherein the residue R6 and R7, are, independently of each other, selected from the group consisting of -H, -D, -alkyl, alkoxy, alkenyl, alkynyl, halides, -NO2, - OH, -NH2, -NHR4#, -CN, - S(O)R4#, -SO2R4#, -P(O)R4#R5#, -P(O)(OR4#)R5#, -P(O)(OR4#)(OR5#), -C(O)NR4#R5#, - C(O)SR4#, -C(O)R4#, -C(O)O-R4#, alkoxy and glycol chains; and wherein R6 may optionally form a cyclic residue, with a further substituent present 5 or 6 position, and wherein R4# and R5# are, independently of each other, selected from the group consisting of -H, -alkyl, -alkenyl, -heterocyclo alkyl, aryl and heteroaryl.
    本发明涉及一种化合物或其在抑制HIV衣壳组装中的药用盐或溶剂中的使用,该化合物包括核心结构,其中E为CR7或S,其中f为0或1,在E为S的情况下,f为0,在核心结构至少在2和4位置被取代,在残基R6和R7中,它们分别选自-H,-D,-烷基,烷氧基,烯基,炔基,卤素,-NO2,-OH,-NH2,-NHR4#,-CN,-S(O)R4#,-SO2R4#,-P(O)R4#R5#,-P(O)(OR4#)R5#,-P(O)(OR4#)(OR5#),-C(O)NR4#R5#,-C(O)SR4#,-C(O)R4#,-C(O)O-R4#,烷氧基和甘醇链;其中R6可以选择形成一个环状残基,并在5或6位置存在另一个取代基,而R4#和R5#分别选自-H,-烷基,-烯基,-杂环烷基,芳基和杂芳基。
  • COMPOUNDS AND THERAPEUTICAL USE THEREOF
    申请人:Cai Xiong Sui
    公开号:US20070244113A1
    公开(公告)日:2007-10-18
    Disclosed are 4-arylamino-quinazolines and analogs thereof effective as activators of caspases and inducers of apoptosis. The compounds of this invention are useful in the treatment of a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.
    本发明揭示了4-芳氨基喹唑啉及其类似物,可有效激活半胱氨酸蛋白酶并诱导细胞凋亡。本发明的化合物在治疗各种临床情况中具有用途,其中异常细胞的不受控制的生长和扩散。
  • Compounds and therapeutical use thereof
    申请人:Cai Xiong Sui
    公开号:US20050137213A1
    公开(公告)日:2005-06-23
    Disclosed are 4-arylamino-quinazolines and analogs thereof effective as activators of caspases and inducers of apoptosis. The compounds of this invention are useful in the treatment of a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.
    本发明揭示了4-芳基氨基喹唑啉及其类似物,它们有效地激活半胱氨酸蛋白酶并诱导细胞凋亡。本发明的化合物在治疗各种临床病症中具有用途,其中发生异常细胞的不受控制的生长和扩散。
  • METHOD OF TREATING BRAIN CANCER
    申请人:Cai Sui Xiong
    公开号:US20080051398A1
    公开(公告)日:2008-02-28
    Disclosed are 4-arylamino-quinazolines and analogs thereof effective as activators of caspases and inducers of apoptosis. The compounds of this invention are useful in the treatment of a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs, and in particular to the use of these compounds in treating brain cancer.
    本发明涉及4-芳基氨基喹唑啉及其类似物,其有效激活caspases并诱导细胞凋亡。本发明的化合物可用于治疗各种临床病症,其中发生异常细胞的不受控制的生长和扩散,特别是用于治疗脑癌。
  • 4-arylamino-quinazolines and analogs as activators of caspases and inducers of apoptosis and the use thereof
    申请人:Myriad Pharmaceuticals, Inc.
    公开号:US07618975B2
    公开(公告)日:2009-11-17
    Disclosed are 4-arylamino-quinazolines and analogs thereof effective as activators of caspases and inducers of apoptosis. The compounds of this invention are useful in the treatment of a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.
    本发明揭示了4-芳基氨基喹唑啉及其类似物,其作为caspase激活剂和诱导凋亡剂具有有效性。本发明的化合物在治疗各种临床病症中有用,其中发生异常细胞的不受控制的生长和扩散。
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