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2-(7-Ethoxynaphthalen-1-yl)ethanamine;hydrochloride

中文名称
——
中文别名
——
英文名称
2-(7-Ethoxynaphthalen-1-yl)ethanamine;hydrochloride
英文别名
2-(7-ethoxynaphthalen-1-yl)ethanamine;hydrochloride
2-(7-Ethoxynaphthalen-1-yl)ethanamine;hydrochloride化学式
CAS
——
化学式
C14H18ClNO
mdl
——
分子量
251.75
InChiKey
ZHGYHJLOPBVMCG-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):
    3.16
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    35.2
  • 氢给体数:
    2
  • 氢受体数:
    2

文献信息

  • [EN] AN IMPROVED PROCESS FOR PREPARATION OF AGOMELATINE<br/>[FR] PROCÉDÉ PERFECTIONNÉ POUR LA PRÉPARATION D'AGOMÉLATINE
    申请人:CADILA HEALTHCARE LTD
    公开号:WO2014072998A1
    公开(公告)日:2014-05-15
    The present invention provides an improved process for preparing agomelatine of formula (I). The process comprises reacting 7-methoxy tetralone with cyanoacetic acid in an organic solvent to obtain (7-methoxy-3,4-dihydro- 1 -naphthalenyl)acetonitrile of Formula (B); treating compound of Formula (B) with a catalyst to obtain (7-methoxy- 1 - naphthyl)acetonitrile of Formula (C); reducing compound of formula (C) with hydrogen in presence of Raney nickel in ammoniacal methanol medium and subsequently converting to a salt using hydrochloric acid to obtain 2-(7-methoxy- 1 -naphthyI)ethanamine hydrochloride of formula (D); iv) reacting compound of formula (D) with acetic anhydride or acetic chloride in an organic solvent in presence of a base and a catalyst to obtain agomelatine of Formula (I); and optionally purifying agomelatine of Formula (I). The present invention also provides a process for preparing polymorphic Form-I of agomelatine of formula (I) comprising treating agomelatine of formula (I) in a suitable organic solvent; and isolating polymorphic Form-I of agomelatine of formula (I).
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