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6-(4-fluorophenyl)ethynyl-2-methylthio-4-pyrrolidin-1-ylpyrimidine-5-carbaldehyde | 1104638-81-4

中文名称
——
中文别名
——
英文名称
6-(4-fluorophenyl)ethynyl-2-methylthio-4-pyrrolidin-1-ylpyrimidine-5-carbaldehyde
英文别名
4-[2-(4-Fluorophenyl)ethynyl]-2-methylsulfanyl-6-pyrrolidin-1-ylpyrimidine-5-carbaldehyde
6-(4-fluorophenyl)ethynyl-2-methylthio-4-pyrrolidin-1-ylpyrimidine-5-carbaldehyde化学式
CAS
1104638-81-4
化学式
C18H16FN3OS
mdl
——
分子量
341.409
InChiKey
GYNHNDXXBTWCEA-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):
    3.6
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    71.4
  • 氢给体数:
    0
  • 氢受体数:
    6

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:
    6-(4-fluorophenyl)ethynyl-2-methylthio-4-pyrrolidin-1-ylpyrimidine-5-carbaldehyde叔丁胺 作用下, 反应 24.0h, 以92%的产率得到7-(4-fluorophenyl)-2-methylthio-4-pyrrolidin-1-ylpyrido[4,3-d]pyrimidine
    参考文献:
    名称:
    An Efficient One-Pot Synthetic Method for 2,4-Disubstituted 7-Arylpyrido[4,3-d]pyrimidines from 2,4-Disubstituted 6-(Arylethynyl)pyrimidine-5-carbaldehydes and tert-Butylamine
    摘要:
    2,4-二取代的6-(芳基-乙炔基)嘧啶-5-甲醛与叔丁胺发生意外的热环化,在不存在的情况下以良好的收率得到2,4-二取代的7-芳基吡啶并[4,3-d]嘧啶任何催化剂。分离了中间体化合物并讨论了可能的反应机理。
    DOI:
    10.1055/s-0028-1083500
  • 作为产物:
    描述:
    4-氟苯乙炔4-氯-2-甲基磺酰基-6-吡咯烷-1-基-嘧啶-5-甲醛 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以82%的产率得到6-(4-fluorophenyl)ethynyl-2-methylthio-4-pyrrolidin-1-ylpyrimidine-5-carbaldehyde
    参考文献:
    名称:
    Study on the cyclization of 6-arylethynylpyrimidine-5-carbaldehydes with tert-butylamine: microwave versus thermal preparation of pyrido[4,3-d]pyrimidines
    摘要:
    Thermal and microwave initiated cyclization of 2,4-disubstituted 6-arylethynylpyrimidine-5-carbaldehydes with tert-butylamine has been studied. A novel high-yielding preparation of 2,4-disubstituted 7-arylpyrido[4,3-d]pyrimidines has been developed. The intermediate compounds were isolated and possible mechanism of the reactions is discussed. Crown Copyright (C) 2009 Published by Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.05.015
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文献信息

  • An Efficient One-Pot Synthetic Method for 2,4-Disubstituted 7-Arylpyrido[4,3-<i>d</i>]pyrimidines from 2,4-Disubstituted 6-(Arylethynyl)pyrimidine-5-carbaldehydes and <i>tert</i>-Butylamine
    作者:Inga Cikotiene、Marius Morkunas、Simonas Rudys、Rita Buksnaitiene、Algirdas Brukstus
    DOI:10.1055/s-0028-1083500
    日期:——
    Unexpected thermal cyclization of 2,4-disubstituted 6-(aryl-ethynyl)pyrimidine-5-carbaldehydes with tert-butylamine proceeded to give 2,4-disubstituted 7-arylpyrido[4,3-d]pyrimidines in good yields in the absence of any catalysts. The intermediate compounds were isolated and possible mechanism of the reactions is discussed.
    2,4-二取代的6-(芳基-乙炔基)嘧啶-5-甲醛与叔丁胺发生意外的热环化,在不存在的情况下以良好的收率得到2,4-二取代的7-芳基吡啶并[4,3-d]嘧啶任何催化剂。分离了中间体化合物并讨论了可能的反应机理。
  • The First and Efficient Synthesis of 7-Aryl-6-methoxycarbonylquinazolines via Unexpected Reaction of 6-Arylethynylpyrimidine-5-carbaldehydes and Methyl Mercaptoacetate
    作者:Inga Cikotiene、Marius Morkunas
    DOI:10.1055/s-0028-1087514
    日期:——
    A highly concise synthesis of 7-aryl-6-methoxycarbonylquinazolines via reaction of 6-arylethynylpyrimidine-5-carbaldehydes and methyl mercaptoacetate is described.
    描述了通过 6-芳基乙炔基嘧啶-5-甲醛和巯基乙酸甲酯的反应高度简洁地合成 7-芳基-6-甲氧基羰基喹唑啉。
  • Study on the cyclization of 6-arylethynylpyrimidine-5-carbaldehydes with tert-butylamine: microwave versus thermal preparation of pyrido[4,3-d]pyrimidines
    作者:Inga Cikotiene、Visvaldas Kairys、Rita Buksnaitiene、Marius Morkunas、Simonas Rudys、Algirdas Brukstus、Miguel X. Fernandes
    DOI:10.1016/j.tet.2009.05.015
    日期:2009.7
    Thermal and microwave initiated cyclization of 2,4-disubstituted 6-arylethynylpyrimidine-5-carbaldehydes with tert-butylamine has been studied. A novel high-yielding preparation of 2,4-disubstituted 7-arylpyrido[4,3-d]pyrimidines has been developed. The intermediate compounds were isolated and possible mechanism of the reactions is discussed. Crown Copyright (C) 2009 Published by Elsevier Ltd. All rights reserved.
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