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(3-amino-6-phenyl-furo[2,3-b]pyridin-2-yl)-(4-nitro-phenyl)-methanone | 54891-74-6

中文名称
——
中文别名
——
英文名称
(3-amino-6-phenyl-furo[2,3-b]pyridin-2-yl)-(4-nitro-phenyl)-methanone
英文别名
(3-Amino-6-phenylfuro[2,3-b]pyridin-2-yl)-(4-nitrophenyl)methanone
(3-amino-6-phenyl-furo[2,3-<i>b</i>]pyridin-2-yl)-(4-nitro-phenyl)-methanone化学式
CAS
54891-74-6
化学式
C20H13N3O4
mdl
——
分子量
359.341
InChiKey
NHBZUUKJKHHEAB-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):
    4.6
  • 重原子数:
    27
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    115
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

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文献信息

  • [EN] FUROPYRIDINE AND FUROPYRIMIDINE DERIVATIVES FOR THE TREATMENT OF HYPER-PROLIFERATIVE DISORDERS<br/>[FR] DERIVES DE FUROPYRIDINE ET DE FUROPYRIMIDINE UTILISES DANS LE TRAITEMENT DE TROUBLES HYPERPROLIFERATIFS
    申请人:BAYER PHARMACEUTICALS CORP
    公开号:WO2004007502A1
    公开(公告)日:2004-01-22
    This invention relates to a compound of Formula (I) wherein Y is CH or N; Ar1 is phenyl or pyridyl each optionally substituted with 1 or 2 substituents each selected independently from (C1-C3)alkoxy halo, OH, CF3, CN, NO2 and (C1-C3)alkyl, said alkyl being optionally substituted with CF3; Ar2 is phenyl or pyridyl each optionally substituted with 1 or 2 substituents each independently selected from halo, OH, CN, NO2, CF3, (C1-C6)alkoxy, NR1R1, S(O)2R2, C(O)R3, and (C1-C6)alkyl optionally substituted with R4, and its use in treating hyper-proliferative disorders.
    这项发明涉及一种化合物,其化学式为(I),其中Y为CH或N;Ar1为苯基或吡啶基,每个基团可选择地取代为1或2个基团,每个基团可独立地从(C1-C3)烷氧基卤素、OH、CF3、CN、NO2和(C1-C3)烷基中选择,所述烷基可选择地取代为 ;Ar2为苯基或吡啶基,每个基团可选择地取代为1或2个基团,每个基团可独立地从卤素、OH、CN、 、 、(C1-C6)烷氧基、NR1R1、S(O)2R2、C(O)R3和(C1-C6)烷基中选择,所述烷基可选择地取代为R4;以及其在治疗过度增殖性疾病中的用途。
  • Furopyridine and furopyrimidine derivatives for the treatment of hyper-proliferative disorders
    申请人:Zhang Chengzhi
    公开号:US20060040960A1
    公开(公告)日:2006-02-23
    This invention relates to a compound of Formula (I) wherein Y is CH or N; Ar 1 is phenyl or pyridyl each optionally substituted with 1 or 2 substituents each selected independently from (C 1 -C 3 )alkoxy halo, OH, CF 3 , CN, NO 2 and (C 1 -C 3 )alkyl, said alkyl being optionally substituted with CF 3 ; Ar 2 is phenyl or pyridyl each option-ally substituted with 1 or 2 substituents each independently selected from halo, OH, CN, NO 2 , CF 3 , (C 1 -C 6 )alkoxy, NR 1 R 1 , S(O) 2 R 2 , C(O)R 3 , and (C 1 -C 6 )alkyl optionally substituted with R 4 , and its use in treating hyper-proliferative disorders.
    本发明涉及化合物式(I),其中Y为CH或N;Ar1为苯基或吡啶基,每个基团可选地取代为1或2个取自(C1-C3)烷氧基,卤素,羟基,三甲基,基,硝基和(C1-C3)烷基的基团,所述烷基可选地取代为三甲基;Ar2为苯基或吡啶基,每个基团可选地取代为1或2个取自卤素,羟基,基,硝基,三甲基,(C1-C6)烷氧基,NR1R1,S(O)2R2,C(O)R3和可选地取代为R4的(C1-C6)烷基的基团,并且该化合物在治疗增生性疾病中的应用。
  • FUROPYRIDINE AND FUROPYRIMIDINE DERIVATIVES FOR THE TREATMENT OF HYPER-PROLIFERATIVE DISORDERS
    申请人:Zhang Chengzhi
    公开号:US20090143412A1
    公开(公告)日:2009-06-04
    This invention relates to a compound of Formula I wherein Y is CH or N; Ar 1 is phenyl or pyridyl each optionally substituted with 1 or 2 substituents each selected independently from (C 1 -C 3 )alkoxy, halo, OH, CF 3 , CN, NO 2 and (C 1 -C 3 )alkyl, said alkyl being optionally substituted with CF 3 ; Ar 2 is phenyl or pyridyl each optionally substituted with 1 or 2 substituents each independently selected from halo, OH, CN, NO 2 , CF 3 , (C 1 -C 6 )alkoxy, NR 1 R 1 , S(O) 2 R 2 , C(O)R 3 , and (C 1 -C 6 )alkyl optionally substituted with R 4 , and its use in treating hyper-proliferative disorder.
    本发明涉及一种化合物I的配合物,其中Y为CH或N;Ar1为苯基或吡啶基,每个基团可选地取代为1或2个基团,每个基团独立地选自(C1-C3)烷氧基,卤素,羟基,三甲基,基,硝基和(C1-C3)烷基,所述烷基可选地取代为三甲基;Ar2为苯基或吡啶基,每个基团可选地取代为1或2个基团,每个基团独立地选自卤素,羟基,基,硝基,三甲基,(C1-C6)烷氧基,NR1R1,S(O)2R2,C(O)R3和可选地取代为R4的(C1-C6)烷基,以及其在治疗高增殖性疾病中的用途。
  • GEWALD K.; JAENSCH H. J., J. PRAKT. CHEM. <JPCE-AO>, 1976, 318, NO 2, 313-320
    作者:GEWALD K.、 JAENSCH H. J.
    DOI:——
    日期:——
  • US7429584B2
    申请人:——
    公开号:US7429584B2
    公开(公告)日:2008-09-30
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