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N-[4-(3-Cyano-benzyl)-morpholin-2-ylmethyl]-acetamide | 112886-98-3

中文名称
——
中文别名
——
英文名称
N-[4-(3-Cyano-benzyl)-morpholin-2-ylmethyl]-acetamide
英文别名
N-[[4-[(3-cyanophenyl)methyl]morpholin-2-yl]methyl]acetamide
N-[4-(3-Cyano-benzyl)-morpholin-2-ylmethyl]-acetamide化学式
CAS
112886-98-3
化学式
C15H19N3O2
mdl
——
分子量
273.335
InChiKey
GHNQPLMOIGTULC-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):
    0.9
  • 重原子数:
    20.0
  • 可旋转键数:
    4.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    65.36
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    N-[4-(3-Cyano-benzyl)-morpholin-2-ylmethyl]-acetamide盐酸 作用下, 反应 4.0h, 生成 3-[[2-(Aminomethyl)morpholin-4-yl]methyl]benzonitrile
    参考文献:
    名称:
    Novel benzamides as selective and potent gastrokinetic agents. 2. Synthesis and structure-activity relationships of 4-amino-5-chloro-2-ethoxy-N-[[4-(4-fluorobenzyl)-2-morpholinyl]methyl]benzamide citrate (AS-4370) and related compounds
    摘要:
    The title compounds (19-55) with a 4-substituted 2-(aminomethyl) morpholine group were prepared and evaluated for the gastrokinetic activity by determining their effect on gastric emptying of phenol red semisolid meal in rats. Introduction of chloro, fluoro, and trifluoromethyl groups to the benzyl group of the parent compounds 1a and 1b enhanced the activity. Among compounds tested, 4-amino-5-chloro-2-ethoxy-N-[[4-(4-fluorobenzyl)-2-morpholinyl]?? methyl]benzamide (23b) showed the most potent gastic emptying activity (effects on phenol red semisolid meal in rats and mice, and on resin pellets solid meal in rats). The gastrokinetic activity of 23b citrate (AS-4370) compared very favorably with that of cisapride and was higher than that of metoclopramide. In contrast to metoclopramide and cisapride, AS-4370 was free from dopamine D2 receptor antagonistic activity in both in vitro ([H-3]spiperone binding) and in vivo (apomorphine-induced emesis in dogs) tests.
    DOI:
    10.1021/jm00106a023
  • 作为产物:
    描述:
    2-(N-acetylaminomethyl)-4-benzylmorpholine 在 palladium on activated charcoal 氢气potassium carbonate溶剂黄146 、 potassium iodide 作用下, 以 乙醇丁酮 为溶剂, 反应 17.0h, 生成 N-[4-(3-Cyano-benzyl)-morpholin-2-ylmethyl]-acetamide
    参考文献:
    名称:
    Novel benzamides as selective and potent gastrokinetic agents. 2. Synthesis and structure-activity relationships of 4-amino-5-chloro-2-ethoxy-N-[[4-(4-fluorobenzyl)-2-morpholinyl]methyl]benzamide citrate (AS-4370) and related compounds
    摘要:
    The title compounds (19-55) with a 4-substituted 2-(aminomethyl) morpholine group were prepared and evaluated for the gastrokinetic activity by determining their effect on gastric emptying of phenol red semisolid meal in rats. Introduction of chloro, fluoro, and trifluoromethyl groups to the benzyl group of the parent compounds 1a and 1b enhanced the activity. Among compounds tested, 4-amino-5-chloro-2-ethoxy-N-[[4-(4-fluorobenzyl)-2-morpholinyl]?? methyl]benzamide (23b) showed the most potent gastic emptying activity (effects on phenol red semisolid meal in rats and mice, and on resin pellets solid meal in rats). The gastrokinetic activity of 23b citrate (AS-4370) compared very favorably with that of cisapride and was higher than that of metoclopramide. In contrast to metoclopramide and cisapride, AS-4370 was free from dopamine D2 receptor antagonistic activity in both in vitro ([H-3]spiperone binding) and in vivo (apomorphine-induced emesis in dogs) tests.
    DOI:
    10.1021/jm00106a023
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