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2-环己基哌啶盐酸盐 | 51523-81-0

中文名称
2-环己基哌啶盐酸盐
中文别名
——
英文名称
2-cyclohexyl-piperidine; hydrochloride
英文别名
2-Cyclohexyl-piperidin; Hydrochlorid;2-Cyclohexylpiperidine hydrochloride;2-cyclohexylpiperidine;hydrochloride
2-环己基哌啶盐酸盐化学式
CAS
51523-81-0
化学式
C11H21N*ClH
mdl
——
分子量
203.755
InChiKey
LOBXPLPVYOYYKM-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):
    3.13
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    12
  • 氢给体数:
    2
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2933399090

SDS

SDS:eecc3e2584feda0886ea6b0fd6ee8b42
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反应信息

  • 作为产物:
    描述:
    2-苯基吡啶盐酸 作用下, 以 乙醇氢气丙酮 为溶剂, 生成 2-环己基哌啶盐酸盐
    参考文献:
    名称:
    3-(Piperidino-lower-alkyl)-indoles
    摘要:
    1-酰基-3-(氨基-较低烷基)吲哚,作为抗炎药物有用,可以通过以下方式制备:通过对3-(氨基-较低烷基)吲哚进行酰化;通过从N'-酰基苯基肼和氨基-较低烷酮进行费舍尔吲哚合成;通过将胺基化合物与1-酰基-3-(卤代-较低烷基)吲哚进行烷基化;或通过还原烷基化1-酰基-3-吲哚-较低烷基羧醛。
    公开号:
    US04021431A1
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文献信息

  • 4-[[3-[.alpha.-Aminobenzyl]phenyl]methyl]morpholine and
    申请人:Sterling Drug Inc.
    公开号:US04308382A1
    公开(公告)日:1981-12-29
    N-2, 3- and 4-[R.sub.1 -(phenyl)-C(=X)]-phenyl-lower-alkyl}amines, useful as anti-inflammatory agents, are prepared either by reduction of 2-, 3- or 4-[R.sub.1 -(phenyl)-CO]-phenyl-lower-alkanoylamines, which are also useful as anti-inflammatory agents; by benzoylating a phenyl-lower-alkylamine; by reaction of a 2-, 3- or 4-lithiophenyl-lower-alkylamine with a R.sub.1 -(phenyl)-carboxaldehyde, a R.sub.1 -(phenyl)-lower-alkyl ketone or a R.sub.1 -(phenyl)-carbonitrile; by reaction of a 2-, 3- or 4-[R.sub.1 -(phenyl)-CO]-phenyl-lower-alkyl tosylate with an appropriate amine; or by transformations involving manipulations of a carbonyl or carbinol group.
    N-2, 3-和4-[R1-(苯基)-C(=X)]-苯基-低碳烷基}胺,作为抗炎药很有用,可以通过还原2-, 3-或4-[R1-(苯基)-CO]-苯基-低碳烷酰胺来制备,这些低碳烷酰胺作为抗炎药也很有效;通过苯甲酰化苯基-低碳烷基胺;通过与R1-(苯基)-甲酰甲醛、R1-(苯基)-低碳烷基酮或R1-(苯基)-腈的2-, 3-或4-锂苯基-低碳烷基胺反应;通过与适当胺的2-, 3-或4-[R1-(苯基)-CO]-苯基-低碳烷基甲磺酸酯反应;或者通过涉及羰基或甲醇基团操纵的转化来制备。
  • Intermediates for preparing anti-inflammatory phenyl-lower-alkylamines
    申请人:Sterling Drug Inc.
    公开号:US04216326A1
    公开(公告)日:1980-08-05
    N-3- and 4-[R.sub.1 -(phenyl)-C(.dbd.X)]-phenyl-lower-alkyl}amines, useful as anti-inflammatory agents, are prepared either by reduction of 3- or 4-[R.sub.1 -(phenyl)-CO]-phenyl-lower-alkanoylamines, which are also useful as anti-inflammatory agents; by benzoylating a phenyl-lower-alkylamine; by reaction of a 3- or 4-lithiophenyl-lower-alkylamine with a R.sub.1 -(phenyl)-carboxaldehyde, a R.sub.1 -(phenyl)-lower-alkyl ketone or a R.sub.1 -(phenyl)-carbonitrile or by transformations involving manipulations of a carbonyl or carbinol group.
    N-3-和4-[R1-(苯基)-C(=X)]-苯基-低碳烷基}胺,作为抗炎药有效,可以通过还原3-或4-[R1-(苯基)-CO]-苯基-低碳烷酰胺制备,后者也作为抗炎药有效;通过苯甲酰化苯基-低碳烷基胺;通过与R1-(苯基)-甲醛、R1-(苯基)-低碳烷基酮或R1-(苯基)-腈的3-或4-锂苯基-低碳烷基胺反应,或者通过涉及羰基或甲醇基团操纵的转化来制备。
  • Anti-inflammatory phenyl-lower-alkylamines
    申请人:Sterling Drug Inc.
    公开号:US04069256A1
    公开(公告)日:1978-01-17
    N-3-[R.sub.1 -(phenyl)-C(=X)]-phenyl-lower-alkyl}amines having anti-inflammatory utility are prepared either by reduction of a 3-[R.sub.1 -(phenyl)-CO]-phenyl-lower-alkanoylamine; by benzoylating a phenyl-lower-alkylamine; by reaction of a 3-lithiophenyl-lower-alkylamine with a R.sub.1 -(phenyl)-carboxaldehyde, a R.sub.1 -(phenyl)lower-alkyl ketone or a R.sub.1 -(phenyl)-carbonitrile or by transformations involving manipulations of a carbonyl or carbinol group.
    具有抗炎活性的N-3-[R₁-(苯基)-C(=X)]-苯基-低碳烷基}胺可以通过以下方式制备:还原3-[R₁-(苯基)-CO]-苯基-低碳烷酰胺;通过苯甲酰化苯基-低碳烷基胺;通过3-锂代苯基-低碳烷基胺与R₁-(苯基)-甲酰甲醛、R₁-(苯基)低碳烷基酮或R₁-(苯基)-碳氰化物的反应;或者通过涉及羰基或甲醇基团操作的转换过程。
  • 1-Acyl-3-(amino-lower-alkyl)indoles
    申请人:Sterling Drug Inc.
    公开号:US04160862A1
    公开(公告)日:1979-07-10
    1-Acyl-3-(amino-lower-alkyl)indoles, useful as anti-inflammatory agents, are prepared either by acylation of a 3-(amino-lower-alkyl)indole; by Fisher indole synthesis from an N'-acylphenylhydrazine and an amino-lower-alkanone; by alkylation of an amine with a 1-acyl-3-(halo-lower-alkyl)indole; or by reductive alkylation of a 1-acyl-3-indole-lower-alkylcarboxaldehyde.
    1-酰基-3-(氨基-低碳烷基)吲哚,可作为抗炎药物,可通过以下方法制备:将3-(氨基-低碳烷基)吲哚酰化;通过N'-酰基苯基腙和氨基-低碳烷酮的菲舍尔吲哚合成;通过胺与1-酰基-3-(卤代-低碳烷基)吲哚的烷基化;或者通过1-酰基-3-吲哚-低碳烷基羰基的还原烷基化。
  • 2-Naphthyl-lower-alkylamines
    申请人:Sterling Drug Inc.
    公开号:US04005093A1
    公开(公告)日:1977-01-25
    2-Naphthyl-lower-alkylamines, useful as anti-inflammatory agents, are prepared by reaction of a 2-naphthyl-lower-alkanoyl halide with an amine and reduction of the resulting 2-naphthyl-lower-alkanoylamine with a reagent effective to reduce an amide to an amine.
    2-萘-较低烷基胺,作为抗炎药物,通过2-萘-较低烷酰卤与胺反应,并使用有效还原酰胺为胺的试剂还原所得的2-萘-较低烷酰胺来制备。
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