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4-(9-isopropyl-9H-purin-6-yl)phenol | 1235035-60-5

中文名称
——
中文别名
——
英文名称
4-(9-isopropyl-9H-purin-6-yl)phenol
英文别名
4-(9-propan-2-ylpurin-6-yl)phenol
4-(9-isopropyl-9H-purin-6-yl)phenol化学式
CAS
1235035-60-5
化学式
C14H14N4O
mdl
——
分子量
254.291
InChiKey
SCRYAZZFTCWFHY-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):
    2.1
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    63.8
  • 氢给体数:
    1
  • 氢受体数:
    4

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

反应信息

  • 作为反应物:
    描述:
    3,5-bis(trifluoromethyl)phenyl azide4-(9-isopropyl-9H-purin-6-yl)phenol 在 silver hexafluoroantimonate 、 dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 12.0h, 以52%的产率得到N-[3,5-bis(trifluoromethyl)phenyl]-5-hydroxy-2-(9-isopropyl-9H-purin-6-yl)aniline
    参考文献:
    名称:
    Hydrogen-Bond-Assisted Controlled C–H Functionalization via Adaptive Recognition of a Purine Directing Group
    摘要:
    We have developed the Rh-catalyzed selective C-H functionalization of 6-arylpurines, in which the purine moiety directs the C-H bond activation of the aryl pendant. While the first C-H amination proceeds via the N1-chelation assistance, the subsequent second C-H bond activation takes advantage of an intramolecular hydrogen-bonding interaction between the initially formed amino group and one nitrogen atom, either N1 or N7, of the purinyl part. Isolation of a rhodacycle intermediate and the substrate variation studies suggest that N1 is the main active site for the C-H functionalization of both the first and second amination in 6-arylpurines, while N7 plays an essential role in controlling the degree of functionalization serving as an intramolecular hydrogen-bonding site in the second amination process. This pseudo-Curtin-Hammett situation was supported by density functional calculations, which suggest that the intramolecular hydrogen-bonding capability helps second amination by reducing the steric repulsion between the first installed ArNH and the directing group.
    DOI:
    10.1021/ja4118472
  • 作为产物:
    描述:
    9-isopropyl-6-(4-(tetrahydro-2H-pyran-2-yloxy)phenyl)-9H-purine盐酸 作用下, 以 1,4-二氧六环 为溶剂, 反应 1.0h, 以94%的产率得到4-(9-isopropyl-9H-purin-6-yl)phenol
    参考文献:
    名称:
    [EN] HETEROCYCLIC COMPOUNDS AND METHODS OF USE
    [FR] COMPOSÉS HÉTÉROCYCLIQUES ET LEURS PROCÉDÉS D'UTILISATION
    摘要:
    在一个方面,本发明提供了一种具有式I的化合物;其中变量X1a、X1b、X1c、X1d、Q、A、R1、B、L、E和下标m和n的含义如本文所述。在另一个方面,本发明提供了包括式I化合物的药物组合物,以及使用式I化合物治疗由Bcl-2抗凋亡蛋白(例如抗凋亡Bcl-xL蛋白)的表达或过度表达所特征的疾病和状况(例如癌症、血小板增多症等)的方法。
    公开号:
    WO2010080503A1
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文献信息

  • HETEROCYCLIC COMPOUNDS AND METHODS OF USE
    申请人:Baell Jonathan Bayldon
    公开号:US20100210622A1
    公开(公告)日:2010-08-19
    In one aspect, the present invention provides for a compound of Formula I in which the variable X 1a , X 1b , X 1c , X 1d , Q, A, R 1 , B, L, E, and the subscripts m and n have the meanings as described herein. In another aspect, the present invention provides for pharmaceutical compositions comprising compounds of Formula I as well as methods for using compounds of Formula I for the treatment of diseases and conditions (e.g., cancer, thrombocythemia, etc) characterized by the expression or over-expression of Bcl-2 anti-apoptotic proteins, e.g., of anti-apoptotic Bcl-x L proteins.
    在一个方面,本发明提供了一种式子为I的化合物,其中变量X1a,X1b,X1c,X1d,Q,A,R1,B,L,E和下标m和n的含义如此处所述。在另一个方面,本发明提供了包含式子I化合物的制药组合物,以及使用式子I化合物治疗由Bcl-2抗凋亡蛋白(例如抗凋亡Bcl-xL蛋白)的表达或过表达所特征的疾病和病状(例如癌症,血小板增多症等)的方法。
  • Heterocyclic compounds and methods of use
    申请人:Genentech, Inc.
    公开号:US08232273B2
    公开(公告)日:2012-07-31
    In one aspect, the present invention provides for a compound of Formula I in which the variable X1a, X1b, X1c, X1d, Q, A, R1, B, L, E, and the subscripts m and n have the meanings as described herein. In another aspect, the present invention provides for pharmaceutical compositions comprising compounds of Formula I as well as methods for using compounds of Formula I for the treatment of diseases and conditions (e.g., cancer, thrombocythemia, etc) characterized by the expression or over-expression of Bcl-2 anti-apoptotic proteins, e.g., of anti-apoptotic Bcl-xL proteins.
    在一个方面,本发明提供了一种公式I的化合物,其中变量X1a、X1b、X1c、X1d、Q、A、R1、B、L、E和下标m和n的含义如此处所述。在另一个方面,本发明提供了包含公式I化合物的制药组合物,以及使用公式I化合物治疗表达或过度表达Bcl-2抗凋亡蛋白(例如抗凋亡Bcl-xL蛋白)的疾病和状况(例如癌症、血小板增多症等)的方法。
  • US8232273B2
    申请人:——
    公开号:US8232273B2
    公开(公告)日:2012-07-31
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