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4-(4-imidazol-1-yl-phenoxy)-3-methyl-1H-pyrazolo[4,3-c]pyridine | 1246347-14-7

中文名称
——
中文别名
——
英文名称
4-(4-imidazol-1-yl-phenoxy)-3-methyl-1H-pyrazolo[4,3-c]pyridine
英文别名
4-(4-imidazol-1-ylphenoxy)-3-methyl-2H-pyrazolo[4,3-c]pyridine
4-(4-imidazol-1-yl-phenoxy)-3-methyl-1H-pyrazolo[4,3-c]pyridine化学式
CAS
1246347-14-7
化学式
C16H13N5O
mdl
——
分子量
291.312
InChiKey
YLZVQZXADWVYLP-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):
    2.5
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    68.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1-(2,4-二氯吡啶-3-基)乙醇 在 sodium hydride 、 一水合肼N-甲基吗啉氧化物 作用下, 以 1,4-二氧六环二氯甲烷 、 mineral oil 为溶剂, 反应 76.25h, 生成 4-(4-imidazol-1-yl-phenoxy)-3-methyl-1H-pyrazolo[4,3-c]pyridine
    参考文献:
    名称:
    [EN] COMPOUNDS
    [FR] COMPOSÉS
    摘要:
    一种具有式(I)的化合物,或其药学上可接受的盐或酯,其中R1选自:芳基;杂环芳基;-NHR3;融合芳基-C4-7-杂环烷基;-CONR4R5;-NHCOR6;-C3-7-环烷基;-O-C3-7-环烷基;-NR3R6;和可选择地取代的-C1-6烷基;其中所述的芳基、杂环芳基、融合芳基-C4-7-杂环烷基和C4-7-杂环烷基均可选择地取代;R2选自氢、芳基、C1-6-烷基、C2-6-烯基、C3-7-环烷基、杂环芳基、C4-7-杂环烷基和卤素,其中所述的C1-6-烷基、C2-6-烯基、芳基、杂环芳基和C4-7-杂环烷基均可选择地取代。进一步涉及制备具有式(I)的化合物的药物组合物、治疗用途和制备方法的其他方面。
    公开号:
    WO2010106333A1
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文献信息

  • HETEROAROMATIC COMPOUNDS AND THEIR USE AS DOPAMINE D1 LIGANDS
    申请人:PFIZER INC.
    公开号:US20140128374A1
    公开(公告)日:2014-05-08
    The present invention provides, in part, compounds of Formula I: and pharmaceutically acceptable salts thereof and N-oxides of the foregoing; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds, salts or N-oxides, and their uses for treating D1-mediated (or D1-associated) disorders including, e.g., schizophrenia (e.g., its cognitive and negative symptoms), cognitive impairment (e.g., cognitive impairment associated with schizophrenia, AD, PD, or pharmacotherapy therapy), ADHD, impulsivity, compulsive gambling, overeating, autism spectrum disorder, MCI, age-related cognitive decline, dementia, RLS, Parkinson's disease, Huntington's chorea, anxiety, depression, MDD, TRD, and bipolar disorder.
    本发明在一定程度上提供了以下式I的化合物:以及这些化合物的药用盐和其N-氧化物;用于制备这些化合物的工艺;用于制备中间体;以及含有这些化合物、盐或N-氧化物的组合物,并且它们用于治疗D1介导(或D1相关)的疾病,包括但不限于精神分裂症(例如其认知和消极症状)、认知障碍(例如与精神分裂症、阿尔茨海默病、帕金森病或药物治疗相关的认知障碍)、注意力缺陷多动障碍(ADHD)、冲动性、强迫性赌博、过度进食、自闭症谱系障碍、轻度认知障碍、年龄相关认知衰退、痴呆症、不宁腿综合征、帕金森病、亨廷顿舞蹈症、焦虑、抑郁症、抑郁障碍、难治性抑郁症和躁郁症。
  • COMPOUNDS
    申请人:Mciver Edward Giles
    公开号:US20100317646A1
    公开(公告)日:2010-12-16
    A compound of formula I, or a pharmaceutically acceptable salt or ester thereof, wherein R 1 is selected from: aryl; heteroaryl; —NHR 3 ; fused aryl-C 4-7 -heterocycloalkyl; —CONR 4 R 5 ; —NHCOR 6 ; —C 3-7 -cycloalkyl; —O—C 3-7 -cycloalkyl; —NR 3 R 6 ; and optionally substituted —C 1-6 alkyl; wherein said aryl, heteroaryl, fused aryl-C 4-7 -heterocycloalkyl and C 4-7 -heterocycloalkyl are each optionally substituted; R 2 is selected from hydrogen, aryl, C 1-6 -alkyl, C 2-6 -alkenyl, C 3-7 -cycloalkyl, heteroaryl, C 4-7 heterocycloalkyl and halogen, wherein said C 1-6 -alkyl, C 2-6 -alkenyl, aryl, heteroaryl and C 4-7 -heterocycloalkyl are each optionally substituted; R 3 is selected from aryl, heteroaryl, C 4-7 -heterocycloalkyl, C 3-7 -cycloalkyl, fused aryl-C 4-7 -heterocycloalkyl and C 1-6 -alkyl, each of which is optionally substituted; R 4 and R 5 are each independently hydrogen, or optionally substituted C 3-7 -cycloalkyl, aryl, heteroaryl, C 1-6 -alkyl or C 3-6 -heterocycloalkyl; or R 4 and R 5 together with the N to which they are attached form a C 3-6 -heterocycloalkyl ring; each R 6 is independently selected from C 1-6 -alkyl, C 3-7 cycloalkyl, C 4-7 -heterocycloalkyl, aryl and heteroaryl, each of which is optionally substituted each R 7 is selected from hydrogen, optionally substituted C 1-6 -alkyl and C 3-7 -cycloalkyl; each of R 8 and R 9 is independently hydrogen or optionally substituted C 1-6 -alkyl; or R 8 and R 9 together with the N to which they are attached form a C 4-6 -heterocycloalkyl; each R 10 is selected from C 3-7 -cycloalkyl and optionally substituted C 1-6 -alkyl; each R 11 is independently selected from C 1-6 -alkyl, C 3-7 -cycloalkyl, C 1-6 alkyl-C 3-7 -cycloalkyl, C 4-7 -heterocycloalkyl, aryl and heteroaryl, each of which is optionally substituted; A is selected from halogen, —NR 4 SO 2 R 5 , —CN, —OR 6 , —NR 4 R 5 , —NR 7 R 11 , hydroxyl, —CF 3 , —CONR 4 R 5 , —NR 4 COR 5 , —NR 7 (CO)NR 4 R 5 , —NO 2 , —CO 2 H, —CO 2 R 6 , —SO 2 R 6 , —SO 2 NR 4 R 5 , —NR 4 COR 5 , —NR 4 COOR 5 , C 1-6 -alkyl and —COR 6 . Further aspects relate to pharmaceutical compositions, therapeutic uses and process for preparing compounds of formula I.
    化合物I的公式,或其药学上可接受的盐或酯,其中R1选自:芳基;杂环芳基;—NHR3;融合的芳基-C4-7-杂环烷基;—CONR4R5;—NHCOR6;—C3-7-环烷基;—O—C3-7-环烷基;—NR3R6;和可选择取代的—C1-6烷基;其中所述的芳基,杂环芳基,融合的芳基-C4-7-杂环烷基和C4-7-杂环烷基均可选择取代;R2选自氢,芳基,C1-6-烷基,C2-6-烯基,C3-7-环烷基,杂环芳基,C4-7-杂环烷基和卤素,其中所述的C1-6-烷基,C2-6-烯基,芳基,杂环芳基和C4-7-杂环烷基均可选择取代;R3选自芳基,杂环芳基,C4-7-杂环烷基,C3-7-环烷基,融合的芳基-C4-7-杂环烷基和C1-6-烷基,每种均可选择取代;R4和R5各自独立地选自氢,或可选择取代的C3-7-环烷基,芳基,杂环芳基,C1-6-烷基或C3-6-杂环烷基;或R4和R5与它们连接的N一起形成C3-6-杂环烷基环;每个R6各自独立地选自C1-6-烷基,C3-7-环烷基,C4-7-杂环烷基,芳基和杂环芳基,每种均可选择取代;每个R7选自氢,可选择取代的C1-6-烷基和C3-7-环烷基;每个R8和R9各自独立地选自氢或可选择取代的C1-6-烷基;或R8和R9与它们连接的N一起形成C4-6-杂环烷基;每个R10选自C3-7-环烷基和可选择取代的C1-6-烷基;每个R11各自独立地选自C1-6-烷基,C3-7-环烷基,C1-6-烷基-C3-7-环烷基,C4-7-杂环烷基,芳基和杂环芳基,每种均可选择取代;A选自卤素,—NR4SO2R5,—CN,—OR6,—NR4R5,—NR7R11,羟基,—CF3,—CONR4R5,—NR4COR5,—NR7(CO)NR4R5,—NO2,—CO2H,—CO2R6,—SO2R6,—SO2NR4R5,—NR4COR5,—NR4COOR5,C1-6-烷基和—COR6。进一步方面涉及公式I化合物的制药组合物,治疗用途和制备过程。
  • US8822494B2
    申请人:——
    公开号:US8822494B2
    公开(公告)日:2014-09-02
  • US9133190B2
    申请人:——
    公开号:US9133190B2
    公开(公告)日:2015-09-15
  • US9527843B2
    申请人:——
    公开号:US9527843B2
    公开(公告)日:2016-12-27
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