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4-chloro-6-(cyclopentyloxy)pyrimidine | 405931-42-2

中文名称
——
中文别名
——
英文名称
4-chloro-6-(cyclopentyloxy)pyrimidine
英文别名
4-chloro-6-cyclopentyloxypyrimidine
4-chloro-6-(cyclopentyloxy)pyrimidine化学式
CAS
405931-42-2
化学式
C9H11ClN2O
mdl
——
分子量
198.652
InChiKey
DQHCEDCSEAGFRM-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):
    2.7
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    35
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    4-chloro-6-(cyclopentyloxy)pyrimidine 、 4-(4-(4-amino-1H-pyrazole-3-carboxamido)phenyl)piperazine-1-carboxylic acid tert-butyl ester 在 溶剂黄146 作用下, 以 为溶剂, 生成
    参考文献:
    名称:
    Rational design of 4-((6-phenoxypyrimidin-4-yl)amino)-N-(4-(piperazin-1-yl)phenyl)-1H-pyrazole-3-carboxamide (LT-540-717) as orally bioavailable FLT3 inhibitor
    摘要:
    we describe the discovery of compound LT-540-717 (32), a potent FLT3 inhibitor (IC50: 0.62 nM), starting from FN-1501. Compound 32 exhibited highly inhibitory activity against several acquired FLT3 mutations including FLT3 (ITD, D835V), FLT3 (ITD, F691L), FLT3 (D835Y) and FLT3 (D835V). Additionally, 32 displayed potent antiproliferative activity against FLT3-mutation driven BaF3 and AML cells. Oral administration
    DOI:
    10.1016/j.ejmech.2023.115448
  • 作为产物:
    描述:
    4,6-二氯嘧啶环戊醇 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 反应 3.5h, 生成 4-chloro-6-(cyclopentyloxy)pyrimidine
    参考文献:
    名称:
    [EN] QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS
    [FR] COMPOSÉ DE QUINUCLIDINE COMME LIGANDS DU RÉCEPTEUR NICOTINIQUE ALPHA-7 DE L'ACÉTYLCHOLINE
    摘要:
    该披露提供了公式I的化合物,包括它们的盐,以及使用这些化合物的组合物和方法。这些化合物是烟碱7受体的配体,可能对治疗中枢神经系统的各种紊乱,特别是情感和神经退行性疾病有用。
    公开号:
    WO2011053292A1
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文献信息

  • [EN] QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS<br/>[FR] COMPOSÉ DE QUINUCLIDINE COMME LIGANDS DU RÉCEPTEUR NICOTINIQUE ALPHA-7 DE L'ACÉTYLCHOLINE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2011053292A1
    公开(公告)日:2011-05-05
    The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic 7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.
    该披露提供了公式I的化合物,包括它们的盐,以及使用这些化合物的组合物和方法。这些化合物是烟碱7受体的配体,可能对治疗中枢神经系统的各种紊乱,特别是情感和神经退行性疾病有用。
  • QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS
    申请人:Cook, II James H.
    公开号:US20090270405A1
    公开(公告)日:2009-10-29
    The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.
    该披露提供了公式I的化合物,包括它们的盐,以及使用这些化合物的组合物和方法。这些化合物是烟碱性α7受体的配体,可能对治疗中枢神经系统的各种疾病,特别是情感和神经退行性疾病,有用。
  • Pyrimidine compounds and their use
    申请人:——
    公开号:US20040077669A1
    公开(公告)日:2004-04-22
    Pyrimidine compounds of formula (1): 1 wherein R 1 is C 3 -C 7 alkynyl optionally substituted with halogen; R 2 and R 3 are independently hydrogen or the like; and R 4 is C 3 -C 7 alkynyloxy optionally substituted with halogen, optionally substituted phenyl, or the like have an excellent pesticidal effect.
    公式(1)的嘧啶化合物:1其中R1是C3-C7炔基,可选地取代卤素; R2和R3分别是氢或类似物; R4是C3-C7炔氧基,可选地取代卤素,可选地取代苯基或类似物,具有优异的杀虫效果。
  • Quinuclidine Compounds as Alpha-7 Nicotinic Acetylcholine Receptor Ligands
    申请人:Cook, II James H.
    公开号:US20100099684A1
    公开(公告)日:2010-04-22
    The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.
    本公开提供公式I的化合物,包括其盐,以及使用这些化合物的组合物和方法。这些化合物是尼古丁α7受体的配体,可能对中枢神经系统的各种疾病,特别是情感和神经退行性疾病的治疗有用。
  • Quinuclidine compounds as alpha-7 nicotinic acetylcholine receptor ligands
    申请人:Bristol-Myers Squibb Company
    公开号:US07863291B2
    公开(公告)日:2011-01-04
    The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.
    该披露提供了公式I的化合物,包括它们的盐以及使用这些化合物的组合物和方法。这些化合物是尼古丁α7受体的配体,可能对治疗中枢神经系统的各种疾病,特别是情感和神经退行性疾病有用。
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