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4-(2-(difluoromethyl)-1H-benzo[d]imidazol-1-yl)-N-(1-(2-(1-ethylpiperidin-4-yl)phenyl)-2-methylpropan-2-yl)-6-morpholino-1,3,5-triazin-2-amine | 1401436-97-2

中文名称
——
中文别名
——
英文名称
4-(2-(difluoromethyl)-1H-benzo[d]imidazol-1-yl)-N-(1-(2-(1-ethylpiperidin-4-yl)phenyl)-2-methylpropan-2-yl)-6-morpholino-1,3,5-triazin-2-amine
英文别名
4-[2-(difluoromethyl)benzimidazol-1-yl]-N-[1-[2-(1-ethylpiperidin-4-yl)phenyl]-2-methylpropan-2-yl]-6-morpholin-4-yl-1,3,5-triazin-2-amine
4-(2-(difluoromethyl)-1H-benzo[d]imidazol-1-yl)-N-(1-(2-(1-ethylpiperidin-4-yl)phenyl)-2-methylpropan-2-yl)-6-morpholino-1,3,5-triazin-2-amine化学式
CAS
1401436-97-2
化学式
C32H40F2N8O
mdl
——
分子量
590.719
InChiKey
OMPYDTIQSINPLK-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):
    6.1
  • 重原子数:
    43
  • 可旋转键数:
    9
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    84.2
  • 氢给体数:
    1
  • 氢受体数:
    10

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

  • 作为产物:
    描述:
    tert-butyl 4-(2-(2-((4-(2-(difluoromethyl)-1H-benzo[d]imidazol-1-yl)-6-morpholino-1,3,5-triazin-2-yl)amino)-2-methylpropyl)phenyl)piperidine-1-carboxylate 在 sodium cyanoborohydride 、 N,N-二异丙基乙胺三氟乙酸 作用下, 以 二氯甲烷乙腈 为溶剂, 反应 3.0h, 生成 4-(2-(difluoromethyl)-1H-benzo[d]imidazol-1-yl)-N-(1-(2-(1-ethylpiperidin-4-yl)phenyl)-2-methylpropan-2-yl)-6-morpholino-1,3,5-triazin-2-amine
    参考文献:
    名称:
    (ALPHA-SUBSTITUTED ARALKYLAMINO AND HETEROARYLALKYLAMINO) PYRIMIDINYL AND 1,3,5-TRIAZINYL BENZIMIDAZOLES, PHARMACEUTICAL COMPOSITIONS THEREOF, AND THEIR USE IN TREATING PROLIFERATIVE DISEASES
    摘要:
    本文提供了(α-取代的芳基氨基或杂环芳基氨基)嘧啶基和1,3,5-三嗪基苯并咪唑类化合物,例如,式I的化合物,以及它们的药物组合物、制备方法,以及作为治疗增殖性疾病的药剂或药物的用途。
    公开号:
    US20120252802A1
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文献信息

  • (Alpha-substituted aralkylamino and heteroarylalkylamino) pyrimidinyl and 1,3,5-triazinyl benzimidazoles, pharmaceutical compositions thereof, and their use in treating proliferative diseases
    申请人:MEI Pharma, Inc.
    公开号:US10064868B2
    公开(公告)日:2018-09-04
    Provided herein are (alpha-substituted aralkylamino or heteroarylalkylamino) pyrimidinyl and 1,3,5-triazinyl benzimidazoles, e.g., a compound of Formula I, and their pharmaceutical compositions, preparation, and use as agents or drugs for treating proliferative diseases.
    本文提供了(α-取代芳烷基氨基或杂芳基烷基氨基)嘧啶基和 1,3,5-三嗪基苯并咪唑,例如,式 I 的化合物,以及它们的药物组合物、制备和作为治疗增殖性疾病的制剂或药物的用途。
  • Combination therapy
    申请人:MEI Pharma, Inc.
    公开号:US11351176B2
    公开(公告)日:2022-06-07
    Provided herein are methods of treating diseases, such as cancer, using a combination therapy. In certain embodiments, the methods comprise administering an effective amount of a phosphoinositide-3-kinase (PI3K) inhibitor and an effective amount of a CD20 inhibitor to a patient.
    本文提供了使用联合疗法治疗疾病(如癌症)的方法。在某些实施方案中,这些方法包括向患者施用有效量的磷酸肌醇-3-激酶(PI3K)抑制剂和有效量的 CD20 抑制剂。
  • (ALPHA-SUBSTITUTED ARALKYLAMINO AND HETEROARYLALKYLAMINO) PYRIMIDINYL AND 1,3,5-TRIAZINYL BENZIMIDAZOLES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND THESE COMPOUNDS FOR USE IN TREATING PROLIFERATIVE DISEASES
    申请人:MEI Pharma, Inc.
    公开号:EP2691384B1
    公开(公告)日:2016-10-26
  • COMBINATION THERAPY
    申请人:MEI Pharma, Inc.
    公开号:US20190201409A1
    公开(公告)日:2019-07-04
    Provided herein are methods of treating diseases, such as cancer, using a combination therapy. In certain embodiments, the methods comprise administering an effective amount of a phosphoinositide-3-kinase (PI3K) inhibitor and an effective amount of a second agent selected from a Bruton tyrosine kinase (BTK) inhibitor, a Bcl-2 inhibitor, an EZH2 inhibitor and a combination thereof to a patient.
  • TREATMENT OF RELAPSED FOLLICULAR LYMPHOMA
    申请人:MEI Pharma, Inc.
    公开号:US20210196725A1
    公开(公告)日:2021-07-01
    Provided herein are methods treating follicular lymphoma (FL) in subjects having early disease progression after immunochemotherapy using a phosphoinositide-3-kinase (PI3K) inhibitor. In certain embodiments, the methods comprise treating FL in subjects having disease progression within 24 months of initiating first-line or subsequent immunochemotherapy using a phosphoinositide-3-kinase (PI3K) inhibitor.
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