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N-[4-(7-Methoxy-4-methyl-3,4-dihydro-phthalazin-1-yl)-phenyl]-acetamide | 223500-32-1

中文名称
——
中文别名
——
英文名称
N-[4-(7-Methoxy-4-methyl-3,4-dihydro-phthalazin-1-yl)-phenyl]-acetamide
英文别名
N-[4-(7-methoxy-4-methyl-3,4-dihydrophthalazin-1-yl)phenyl]acetamide
N-[4-(7-Methoxy-4-methyl-3,4-dihydro-phthalazin-1-yl)-phenyl]-acetamide化学式
CAS
223500-32-1
化学式
C18H19N3O2
mdl
——
分子量
309.368
InChiKey
GUJYVODUXYUBMI-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):
    2.9
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    62.7
  • 氢给体数:
    2
  • 氢受体数:
    4

上下游信息

  • 下游产品
    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-(7-Methoxy-4-methyl-3,4-dihydro-phthalazin-1-yl)-phenyl]-acetamidesodium hydroxide 作用下, 以 甲醇二氯甲烷 为溶剂, 生成 4-(4-Amino-phenyl)-6-methoxy-1-methyl-1H-phthalazine-2-carboxylic acid ethylamide
    参考文献:
    名称:
    Allosteric modulators of the ampa receptor: Novel 6-substituted dihydrophthalazines
    摘要:
    Novel analogs of the allosteric AMPA receptor modulator SYM 2206 have been prepared. Structure/activity correlations of these novel analogs and other dihydrophthalazines (DHPs) reveal the important contribution of the heteroatom-based aryl substituents in this class of noncompetitive inhibitors. One of the analogs (6, SYM 2189) is equipotent with the early series, but with reduced sedation. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00044-x
  • 作为产物:
    描述:
    4-(Benzhydrylidene-amino)-N-methoxy-N-methyl-benzamide 在 正丁基锂盐酸肼四甲基乙二胺 作用下, 以 四氢呋喃甲醇氯仿 为溶剂, 反应 2.0h, 生成 N-[4-(7-Methoxy-4-methyl-3,4-dihydro-phthalazin-1-yl)-phenyl]-acetamide
    参考文献:
    名称:
    Allosteric modulators of the ampa receptor: Novel 6-substituted dihydrophthalazines
    摘要:
    Novel analogs of the allosteric AMPA receptor modulator SYM 2206 have been prepared. Structure/activity correlations of these novel analogs and other dihydrophthalazines (DHPs) reveal the important contribution of the heteroatom-based aryl substituents in this class of noncompetitive inhibitors. One of the analogs (6, SYM 2189) is equipotent with the early series, but with reduced sedation. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00044-x
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文献信息

  • [DE] PHTHALAZINDERIVATE, DEREN HERSTELLUNG UND VERWENDUNG ALS ARZNEIMITTEL<br/>[EN] PHTHALAZINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS DRUGS<br/>[FR] DERIVES DE PHTALAZINE, LEUR FABRICATION ET LEUR UTILISATION COMME MEDICAMENTS
    申请人:SCHERING AKTIENGESELLSCHAFT
    公开号:WO1997040020A1
    公开(公告)日:1997-10-30
    (DE) Es werden Verbindungen der Formel (I), deren Herstellung und Verwendung als Arzneimittel beschrieben.(EN) Described are compounds of formula (I), their preparation and their use as drugs.(FR) L'invention concerne des composés de la formule (I), leur fabrication et leur utilisation comme médicaments.
    该化合物的式样(I)及其合成与使用情况已被描述。
  • Allosteric modulators of the ampa receptor: Novel 6-substituted dihydrophthalazines
    作者:Xue-Feng Pei、Michael A. Sturgess、C.Fernando Valenzuela、Maria-Luisa Maccecchini
    DOI:10.1016/s0960-894x(99)00044-x
    日期:1999.2
    Novel analogs of the allosteric AMPA receptor modulator SYM 2206 have been prepared. Structure/activity correlations of these novel analogs and other dihydrophthalazines (DHPs) reveal the important contribution of the heteroatom-based aryl substituents in this class of noncompetitive inhibitors. One of the analogs (6, SYM 2189) is equipotent with the early series, but with reduced sedation. (C) 1999 Elsevier Science Ltd. All rights reserved.
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