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1-(3-Methylpiperidin-4-yl)-1,3-dihydro-2H-benzimidazol-2-one | 92309-56-3

中文名称
——
中文别名
——
英文名称
1-(3-Methylpiperidin-4-yl)-1,3-dihydro-2H-benzimidazol-2-one
英文别名
3-(3-methylpiperidin-4-yl)-1H-benzimidazol-2-one
1-(3-Methylpiperidin-4-yl)-1,3-dihydro-2H-benzimidazol-2-one化学式
CAS
92309-56-3
化学式
C13H17N3O
mdl
——
分子量
231.29
InChiKey
KFHJGGBPUGTYQD-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):
    1.3
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    44.4
  • 氢给体数:
    2
  • 氢受体数:
    2

文献信息

  • Phenoxyalkylamine derivatives useful as opioid receptor agonists
    申请人:——
    公开号:US20030171370A1
    公开(公告)日:2003-09-11
    A medicament useful for preventive and/or therapeutic treatment of nerve system diseases which comprises, as an active ingredient, a compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof: 1 wherein, X represents a group represented by the following general formula (II), (III), (IV), (V), or (VI), 2 “A” represents a saturated or unsaturated 3- to 6-membered carbocyclic group and the like, “B” represents CH 2 and the like, “n” represents 0 to 2, R 1 represents a hydrogen atom, a halogen atom and the like, R 2 , R 3 , and R 7 to R 14 represent a hydrogen atom, a lower alkyl group which may be substituted and the like, R 4 represents a hydrogen atom, a lower alkyl group which may be substituted and the like, R 5 represents a hydrogen atom, a halogen atom and the like, R 6 represents a saturated or unsaturated monocyclic or bicyclic carbocyclic group and the like, and R 5 and R 6 , R 7 and R 8 , R 9 and R 10 , or R 11 and R 12 may bind to each other to form a cyclic structure.
    一种用于预防和/或治疗神经系统疾病的药物,其活性成分为以下通用式(I)或其药理学可接受的盐所代表的化合物: 其中,X代表以下通用式(II)、(III)、(IV)、(V)或(VI)所代表的基团,“A”代表饱和或不饱和的3-至6-成员碳环基团等,“B”代表CH2等,“n”代表0至2,R1代表氢原子、卤素原子等,R2、R3和R7至R14代表氢原子、可能被取代的较低烷基基团等,R4代表氢原子、可能被取代的较低烷基基团等,R5代表氢原子、卤素原子等,R6代表饱和或不饱和的单环或双环碳环基团等,且R5和R6、R7和R8、R9和R10,或R11和R12可以结合在一起形成环状结构。
  • Phenoxyalkylamine derivatives useful as opioid delta receptor ligands
    申请人:Tsushima Masaki
    公开号:US20050148583A1
    公开(公告)日:2005-07-07
    A medicament useful for preventive and/or therapeutic treatment of nerve system diseases which comprises, as an active ingredient, a compound represented by the following general formula (I) or a pharmacologically acceptable salt thereof: wherein, X represents a group represented by the following general formula (II), (III), (IV), (V), or (VI), “A” represents a saturated or unsaturated 3- to 6-membered carbocyclic group and the like, “B” represents CH 2 and the like, “n” represents 0 to 2, R 1 represents a hydrogen atom, a halogen atom and the like, R 2 , R 3 , and R 7 to R 14 represent a hydrogen atom, a lower alkyl group which may be substituted and the like, R 4 represents a hydrogen atom, a lower alkyl group which may be substituted and the like, R 5 represents a hydrogen atom, a halogen atom and the like, R 6 represents a saturated or unsaturated monocyclic or bicyclic carbocyclic group and the like, and R 5 and R 6 , R 7 and R 8 , R 9 and R 10 , or R 11 and R 12 may bind to each other to form a cyclic structure.
    一种用于神经系统疾病的预防和/或治疗的药物,其包括以下通式(I)所表示的化合物或其药学上可接受的盐作为活性成分: 其中,X代表以下通式(II),(III),(IV),(V)或(VI)所表示的基团,“A”代表饱和或不饱和的3-至6-成员的碳环基团等,“B”代表CH2等,“n”代表0至2,“R1”代表氢原子,卤原子等,“R2”,“R3”和“R7”至“R14”代表氢原子,可被取代的较低烷基基团等,“R4”代表氢原子,可被取代的较低烷基基团等,“R5”代表氢原子,卤原子等,“R6”代表饱和或不饱和的单环或双环碳环基团等,“R5”和“R6”,“R7”和“R8”,“R9”和“R10”,或“R11”和“R12”可以结合在一起形成环状结构。
  • 2-OXOIMIDAZOLE DERIVATIVES
    申请人:BANYU PHARMACEUTICAL CO., LTD.
    公开号:EP0990653A1
    公开(公告)日:2000-04-05
    The present invention relates to a compound represented by Formula [I] [wherein represents an aromatic carbo- or heterocyclic ring which may have a substituent; Cy represents a mono-, bi- or tricyclic aliphatic carbocyclic group having 3 to 20 carbon atoms, which may have a substituent; represents a mono- or bicyclic aliphatic nitrogen-containing heterocyclic group having 3 to 14 carbon atoms, which may have a substituent; R1 represents a hydrogen atom, a lower alkenyl group, a lower alkynyl group, a cyclo(lower alkyl) group, an amino group, a lower alkylamino group, a di(lower alkyl)amino group, a hydroxyl group, a lower alkoxy group, a carboxyl group, a lower alkoxycarbonyl group, a carbamoyl group, a lower alkylcarbamoyl group or a di(lower alkyl)carbamoyl group, or a lower alkyl group which may have a substituent; and R 2 represents a hydrogen atom or a lower alkyl group], a salt or ester thereof, a production process for the same, and an analgesic, a reliever against tolerance to a narcotic analgesic represented by morphine, a reliever against dependence on a narcotic analgesic represented by morphine, an analgesic enhancer, an antiobestic, a drug for ameliorating brain function, a remedy for schizophrenia, a remedy for Parkinsonism, a remedy for chorea, an antidepressant, a remedy for diabetes insipidus, a remedy for polyuria, or a remedy for hypotension, comprising an effective ingredient of the same.
    本发明涉及一种由式[I]表示的化合物 其中 代表芳香族碳环或杂环,可以有取代基; Cy 代表具有 3 至 20 个碳原子的单环、双环或三环脂族碳环基团,可以有取代基; 代表具有 3 至 14 个碳原子的单环或双环脂族含氮杂环基团,该基团可具有取代基;R1 代表氢原子、低级烯基、低级炔基、环(低级烷基)基团、基、低级烷基基、二(低级烷基)基、羟基、低级烷氧基、羧基、低级烷氧羰基、基甲酰基、低级烷基基甲酰基或二(低级烷基)基甲酰基,或可带有取代基的低级烷基;以及 R 2 代表氢原子或低级烷基],其盐或酯,其生产工艺,以及一种镇痛剂、一种防止对以吗啡为代表的麻醉性镇痛剂产生耐受性的缓解剂、一种防止对以吗啡为代表的麻醉性镇痛剂产生依赖性的缓解剂、一种镇痛增强剂、一种抗抑郁剂、一种改善脑功能的药物、一种治疗精神分裂症的药物、一种治疗帕森病的药物、一种治疗舞蹈症的药物、一种抗抑郁剂、一种治疗糖尿病的药物、一种治疗多尿症的药物或一种治疗低血压的药物,其中包括一种有效成分。
  • PHENOXYALKYLAMINE DERIVATIVES USEFUL AS OPIOID DELTA RECEPTOR AGONISTS
    申请人:Meiji Seika Kaisha, Ltd.
    公开号:EP1256575B1
    公开(公告)日:2005-08-17
  • US6258825B1
    申请人:——
    公开号:US6258825B1
    公开(公告)日:2001-07-10
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