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ethyl 4-piperidylcarbamate hydrochloride | 64951-38-8

中文名称
——
中文别名
——
英文名称
ethyl 4-piperidylcarbamate hydrochloride
英文别名
Ethyl piperidin-4-ylcarbamate hydrochloride;ethyl N-piperidin-4-ylcarbamate;hydrochloride
ethyl 4-piperidylcarbamate hydrochloride化学式
CAS
64951-38-8
化学式
C8H16N2O2*ClH
mdl
MFCD13196158
分子量
208.688
InChiKey
IGQCSJIZVBFKJX-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):
    -0.19
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.875
  • 拓扑面积:
    50.4
  • 氢给体数:
    3
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1-(4-氟苄基)-2-氯苯并咪唑ethyl 4-piperidylcarbamate hydrochloridesodium hydroxidesodium methylate 作用下, 以 甲醇 为溶剂, 生成 咪唑斯汀 、 Ethyl[1-{1-[(4-fluorophenyl)-methyl]-1H-benzimidazol-2-yl}-4-piperidyl]carbamate
    参考文献:
    名称:
    Benzimidazole derivatives and pharmaceutical compositions containing them
    摘要:
    对应于公式(1)的苯并咪唑衍生物 ##STR1## 其中X为CH或N,R.sub.1为氢原子或苯甲基基团,可以承受1至3个取自卤素原子和三氟甲基,(C.sub.1-4)烷基,(C.sub.1-4)烷氧基,氰基,甲硫基,甲基磺酰氧基和甲基磺基基团的取代基,或者带有杂环取代基的甲基基团,在杂环系统中,杂环可以是吡啶基,噻吩基或呋喃基,可以承受一个或多个取代基,R.sub.2为氢原子或(C.sub.1-4)烷基基团,R.sub.3为氢原子或羟基基团,R.sub.4为氢原子或(C.sub.1-4)烷基基团,必要时,当R.sub.3为OH时,以互变异构体的形式存在。这些化合物可用于治疗过敏和组胺引起的炎症。
    公开号:
    US04820710A1
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文献信息

  • 2-[4-pyrimidin-2-yl amino)piperidin-1-yl]benzimidazole compound
    申请人:Synthelabo
    公开号:US04912219A1
    公开(公告)日:1990-03-27
    Benzimidazole derivatives corresponding to the formula (I) ##STR1## in which X is CH or N, R.sub.1 is either a hydrogen atom, or a benzyl radical which can bear 1 to 3 substituents chosen from halogen atoms and trifluoromethyl, (C.sub.1-4)alkyl, (C.sub.1-4)alkoxy, cyano, methylthio, methylsulphinyl and methylsulphonyl radicals, or a methyl radical bearing a heterocyclic substituent in which the heterocyclic system can be a pyridyl, thienyl or furyl radical and can bear one or more substituents, R.sub.2 is a hydrogen atom or a (C.sub.1-4)alkyl radical, R.sub.3 is a hydrogen atom or a hydroxy radical, and R.sub.4 is a hydrogen atom or a (C.sub.1-4)alkyl radical, where appropriate, in tautomeric form when R.sub.3 is OH. The compounds may be used in treating allergy and histamine-induced inflammation.
    公式(I)对应的苯并咪唑衍生物为:##STR1## 其中X为CH或N,R.sub.1为氢原子或苄基基团,该基团可以承载1至3个取自卤素原子和三氟甲基,(C.sub.1-4)烷基,(C.sub.1-4)氧烷基,氰基,甲硫基,甲基磺酰基和甲基磺基基团的取代基,或者带有杂环取代基的甲基基团,其中杂环系统可以是吡啶基,噻吩基或呋喃基,可以承载一个或多个取代基,R.sub.2为氢原子或(C.sub.1-4)烷基基团,R.sub.3为氢原子或羟基基团,R.sub.4为氢原子或(C.sub.1-4)烷基基团,在R.sub.3为OH时,适当时以互变异构体的形式存在。这些化合物可用于治疗过敏和组胺诱导的炎症。
  • US4820710A
    申请人:——
    公开号:US4820710A
    公开(公告)日:1989-04-11
  • US4912219A
    申请人:——
    公开号:US4912219A
    公开(公告)日:1990-03-27
  • Benzimidazole derivatives and pharmaceutical compositions containing them
    申请人:Synthelabo
    公开号:US04820710A1
    公开(公告)日:1989-04-11
    Benzimidazole derivatives corresponding to the formula (1) ##STR1## in which X is CH or N, R.sub.1 is either a hydrogen atom, or a benzyl radical which can bear 1 to 3 substituents chosen from halogen atoms and trifluoromethyl, (C.sub.1-4)alkyl, (C.sub.1-4)alkoxy, cyano, methylthio, methylsulphinyl and methylsulphonyl radicals, or a methyl radical bearing a heterocyclic substituent in which the heterocyclic system can be a pyridyl, thienyl or furyl radical and can bear one or more substituents, R.sub.2 is a hydrogen atom or a (C.sub.1-4)alkyl radical, R.sub.3 is a hydrogen atom or a hydroxy radical, and R.sub.4 is a hydrogen atom or a (C.sub.1-4)alkyl radical, where appropriate, in tautomeric form when R.sub.3 is OH. The compounds may be used in treating allergy and histamine-induced inflammation.
    对应于公式(1)的苯并咪唑衍生物 ##STR1## 其中X为CH或N,R.sub.1为氢原子或苯甲基基团,可以承受1至3个取自卤素原子和三氟甲基,(C.sub.1-4)烷基,(C.sub.1-4)烷氧基,氰基,甲硫基,甲基磺酰氧基和甲基磺基基团的取代基,或者带有杂环取代基的甲基基团,在杂环系统中,杂环可以是吡啶基,噻吩基或呋喃基,可以承受一个或多个取代基,R.sub.2为氢原子或(C.sub.1-4)烷基基团,R.sub.3为氢原子或羟基基团,R.sub.4为氢原子或(C.sub.1-4)烷基基团,必要时,当R.sub.3为OH时,以互变异构体的形式存在。这些化合物可用于治疗过敏和组胺引起的炎症。
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