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5-(4-Fluorophenyl)pyrimidine-2-carboxylic acid

中文名称
——
中文别名
——
英文名称
5-(4-Fluorophenyl)pyrimidine-2-carboxylic acid
英文别名
5-(4-fluorophenyl)-2-pyrimidinecarboxylic acid
5-(4-Fluorophenyl)pyrimidine-2-carboxylic acid化学式
CAS
——
化学式
C11H7FN2O2
mdl
——
分子量
218.187
InChiKey
BUIWLIHYYPTAQQ-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):
    1.8
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    63.1
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    5-(4-Fluorophenyl)pyrimidine-2-carboxylic acid草酰氯三乙胺N,N-二甲基甲酰胺 作用下, 以 四氢呋喃乙腈 为溶剂, 反应 22.0h, 生成
    参考文献:
    名称:
    杂芳酰胺类化合物及其用途
    摘要:
    本发明提供了式Ⅰ所示的化合物及其制备方法,其中R1、R2、R3和R4的定义如说明书所述。本发明式Ⅰ所示的化合物用于肿瘤的治疗。
    公开号:
    CN108623532A
  • 作为产物:
    参考文献:
    名称:
    Imidazopyridine Derivatives
    摘要:
    该发明提供了由通式[I]表示的咪唑吡啶衍生物 [其中R1和R2可能相同或不同,且代表C1-6烷基或类似物,R3和R4代表氢原子,甲基基团或类似物,W代表单环或双环的3-8元芳香或脂肪杂环或类似物,Ar代表可选择取代的芳香杂环或类似物]。这些化合物作为黑色素浓集激素受体拮抗剂,可用于治疗中枢神经系统疾病、心血管系统疾病和代谢性疾病的药物。
    公开号:
    US20080200494A1
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文献信息

  • Imidazopyridine Derivatives
    申请人:Kishino Hiroyuki
    公开号:US20080200494A1
    公开(公告)日:2008-08-21
    The invention provides imidazopyridine derivatives represented by the general formula [I] [in which R 1 and R 2 may be the same or different and stand for C 1-6 alkyl or the like, R 3 and R 4 stand for hydrogen atom, methyl group or the like, W stands for mono- or bi-cyclic 3- to 8-membered aromatic or aliphatic heterocycle or the like, and Ar stands for optionally substituted aromatic heterocycle or the like]. These compounds act as melanin-concentrating hormone receptor antagonist and are useful as medicines for central nervous system disorders, cardiovascular system disorders and metabolic disorders.
    该发明提供了由通式[I]表示的咪唑吡啶衍生物 [其中R1和R2可能相同或不同,且代表C1-6烷基或类似物,R3和R4代表氢原子,甲基基团或类似物,W代表单环或双环的3-8元芳香或脂肪杂环或类似物,Ar代表可选择取代的芳香杂环或类似物]。这些化合物作为黑色素浓集激素受体拮抗剂,可用于治疗中枢神经系统疾病、心血管系统疾病和代谢性疾病的药物。
  • 2-Aminoquinoline derivatives
    申请人:Moriya Minoru
    公开号:US20060287340A1
    公开(公告)日:2006-12-21
    This invention provides 2-aminoquinoline derivatives represented by a general formula [I] [in which R 1 and R 2 either stand for lower alkyl, lower cycloalkyl, etc., or R 1 and R 2 together form an aliphatic nitrogen-containing heterocycle with the nitrogen atom to which they bind; R 3 , R 4 , R 5 , R 6 and R 7 stand for hydrogen, lower alkyl, etc.; R 8 stands for lower alkyl, lower alkyloxy, etc.; and n stands for an integer of 0-4]. The compounds act as melanin concentrating hormone receptor antagonist, and are useful as medicines for central nervous system disorders, cardiovascular disorders and metabolic disorders.
    本发明提供了由通式[I]表示的2-氨基喹啉衍生物[其中R1和R2代表低碳基、低环烷基等,或者R1和R2共同形成一个与它们结合的氮杂环的脂肪族氮杂环;R3、R4、R5、R6和R7代表氢、低碳基等;R8代表低碳基、低碳基氧杂基等;n代表0-4的整数]。这些化合物作为黑色素浓集激素受体拮抗剂,并且可用于治疗中枢神经系统疾病、心血管疾病和代谢性疾病。
  • Imidazopyridine derivatives
    申请人:Banyu Pharmaceuticals, Co., Ltd.
    公开号:US07504412B2
    公开(公告)日:2009-03-17
    The invention provides imidazopyridine derivatives represented by the general formula [I] [in which R1 and R2 may be the same or different and stand for C1-6 alkyl or the like, R3 and R4 stand for hydrogen atom, methyl group or the like, W stands for mono- or bi-cyclic 3- to 8-membered aromatic or aliphatic heterocycle or the like, and Ar stands for optionally substituted aromatic heterocycle or the like]. These compounds act as melanin-concentrating hormone receptor antagonist and are useful as medicines for central nervous system disorders, cardiovascular system disorders and metabolic disorders.
    本发明提供了由通式[I]表示的咪唑吡啶衍生物 [其中R1和R2可以相同或不同,代表C1-6烷基或类似物,R3和R4代表氢原子,甲基基团或类似物,W代表单环或双环3-8成员的芳香或脂肪族杂环或类似物,Ar代表可选取代的芳香杂环或类似物]。这些化合物作为黑素浓聚激素受体拮抗剂,并且可用于治疗中枢神经系统疾病、心血管系统疾病和代谢性疾病的药物。
  • 2-AMINOQUINOLINE DERIVATIVE
    申请人:BANYU PHARMACEUTICAL CO., LTD.
    公开号:EP1630162A1
    公开(公告)日:2006-03-01
    This invention provides 2-aminoquinoline derivatives represented by a general formula [I] [in which R1 and R2 either stand for lower alkyl, lower cycloalkyl, etc., or R1 and R2 together form an aliphatic nitrogen-containing heterocycle with the nitrogen atom to which they bind; R3, R4, R5, R6 and R7 stand for hydrogen, lower alkyl, etc.; R8 stands for lower alkyl, lower alkyloxy, etc.; and n stands for an integer of 0 - 4]. The compounds act as melanin concentrating hormone receptor antagonist, and are useful as medicines for central nervous system disorders, cardiovascular disorders and metabolic disorders.
    本发明提供由通式 [I] 表示的 2-氨基喹啉衍生物 [其中R1和R2代表低级烷基、低级环烷基等,或者R1和R2与它们结合的氮原子一起形成脂肪族含氮杂环;R3、R4、R5、R6和R7代表氢、低级烷基等;R8代表低级烷基、低级烷氧基等;n代表0-4的整数]。这些化合物具有黑色素浓缩激素受体拮抗剂的作用,可作为治疗中枢神经系统疾病、心血管疾病和代谢紊乱的药物。
  • IMIDAZOPYRIDINE DERIVATIVES
    申请人:BANYU PHARMACEUTICAL CO., LTD.
    公开号:EP1657242A1
    公开(公告)日:2006-05-17
    The invention provides imidazopyridine derivatives represented by the general formula [I] [in which R1 and R2 may be the same or different and stand for C1-6 alkyl or the like, R3 and R4 stand for hydrogen atom, methyl group or the like, W stands for mono- or bi-cyclic 3- to 8-membered aromatic or aliphatic heterocycle or the like, and Ar stands for optionally substituted aromatic heterocycle or the like]. These compounds act as melanin-concentrating hormone receptor antagonist and are useful as medicines for central nervous system disorders, cardiovascular system disorders and metabolic disorders.
    本发明提供由通式[I]代表的咪唑吡啶衍生物[其中 R1 和 R2 可以相同或不同,代表 C1-6 烷基或类似物,R3 和 R4 代表氢原子、甲基或类似物,W 代表单环或双环 3 至 8 元芳香族或脂肪族杂环或类似物,Ar 代表任选取代的芳香族杂环或类似物]。这些化合物具有黑色素浓缩激素受体拮抗剂的作用,可作为治疗中枢神经系统疾病、心血管系统疾病和代谢紊乱的药物。
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