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(2'S)-2,2-dimethyl-5-hydroxy-7-pentyl-4-(2'-hydroxypropylimino)-4H-2,3-dihydrobenzopyran | 88879-96-3

中文名称
——
中文别名
——
英文名称
(2'S)-2,2-dimethyl-5-hydroxy-7-pentyl-4-(2'-hydroxypropylimino)-4H-2,3-dihydrobenzopyran
英文别名
4-[(2S)-2-hydroxypropyl]imino-2,2-dimethyl-7-pentyl-3H-chromen-5-ol
(2'S)-2,2-dimethyl-5-hydroxy-7-pentyl-4-(2'-hydroxypropylimino)-4H-2,3-dihydrobenzopyran化学式
CAS
88879-96-3
化学式
C19H29NO3
mdl
——
分子量
319.444
InChiKey
OKURTQCJMLLIAG-ZDUSSCGKSA-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

物化性质

  • 沸点:
    445.8±45.0 °C(Predicted)
  • 密度:
    1.10±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.63
  • 拓扑面积:
    62
  • 氢给体数:
    2
  • 氢受体数:
    4

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

  • 作为产物:
    描述:
    S-1-氨基-2-丙醇4H-1-苯并吡喃-4-酮,2,3-二氢-5-羟基-2,2-二甲基-7-戊基-乙醇 为溶剂, 以77%的产率得到(2'S)-2,2-dimethyl-5-hydroxy-7-pentyl-4-(2'-hydroxypropylimino)-4H-2,3-dihydrobenzopyran
    参考文献:
    名称:
    Synthesis and anticonvulsant and sedative-hypnotic activity of 4-(alkylimino)-2,3-dihydro-4H-1-benzopyrans and benzothiopyrans
    摘要:
    A series of 4-(alkylimino)-5-hydroxy-7-alkyl-2,3-dihydro-4H-1-benzopyrans and -thiopyrans were synthesized and evaluated for anticonvulsant activity. Preliminary screening of these compounds revealed that 2,2-dimethyl-4-[(2-hydroxyalkyl)imino]-5-hydroxy-7-pentyl-2,3- dihydro-4H-1-benzopyrans 19 and 29, the 7-butyl analogue 34, and the corresponding 7-pentyl-4H-1-benzothiopyrans 38 and 39 had the most promising anticonvulsant activity. Synthesis of both enantiomers of 29 and 39 indicated that the R isomers 30 and 40 were the most active and showed very good protection against MES, pentylenetetrazole, and mercaptopropionic acid induced seizures after oral administration in mice. In the Irwin test these compounds showed a generalized depressant activity but at dosages higher than those showing anticonvulsant activity, whereas acute toxicity after oral administration was low (LD50 higher than 400 mg/kg).
    DOI:
    10.1021/jm00172a030
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