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2-乙酰基-4,5-二氯-3(2H)-哒嗪 | 155164-63-9

中文名称
2-乙酰基-4,5-二氯-3(2H)-哒嗪
中文别名
——
英文名称
2-acetyl-4,5-dichloropyridazin-3(2H)-one
英文别名
4,5-Dichloro-2-acetyl-3(2H)-pyridazinone;2-acetyl-4,5-dichloropyridazin-3-one
2-乙酰基-4,5-二氯-3(2H)-哒嗪化学式
CAS
155164-63-9
化学式
C6H4Cl2N2O2
mdl
——
分子量
207.016
InChiKey
RFVTVWCEUKOOFY-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

物化性质

  • 沸点:
    252.1±50.0 °C(Predicted)
  • 密度:
    1.61±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    49.7
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:9e1b6933d503aa2b9b606eb4615152c8
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反应信息

  • 作为反应物:
    描述:
    聚甘氨酸2-乙酰基-4,5-二氯-3(2H)-哒嗪四氢呋喃 为溶剂, 反应 4.0h, 以84%的产率得到N-乙酰甘氨酸
    参考文献:
    名称:
    2-Acylpyridazin-3-ones:用于胺的新型温和化学选择性酰化剂
    摘要:
    2-Acyl-4,5-dichloropyridazin-3-ones 在有机溶剂中的中性条件下可作为胺类的新型 N-酰化试剂。它们是方便、化学选择性和易于处理的稳定的胺 N-酰化试剂。
    DOI:
    10.1055/s-2002-25760
  • 作为产物:
    描述:
    4,5-二氯-3-羟基哒嗪乙酰氯三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 0.08h, 以97%的产率得到2-乙酰基-4,5-二氯-3(2H)-哒嗪
    参考文献:
    名称:
    2-Acylpyridazin-3-ones:用于胺的新型温和化学选择性酰化剂
    摘要:
    2-Acyl-4,5-dichloropyridazin-3-ones 在有机溶剂中的中性条件下可作为胺类的新型 N-酰化试剂。它们是方便、化学选择性和易于处理的稳定的胺 N-酰化试剂。
    DOI:
    10.1055/s-2002-25760
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文献信息

  • Rapid and Ecofriendly Esterification of Alcohols with 2-Acylpyridazinones
    作者:Bo Ram Kim、Gi Hyeon Sung、Ki Eun Ryu、Jeum-Jong Kim、Yong-Jin Yoon
    DOI:10.5012/bkcs.2013.34.11.3410
    日期:2013.11.20
    Atom-economical esterification is of great importance in green chemistry. In this work, we demonstrated the catalyst and additive free esterification of alcohols by their reaction with 2-acyl-4,5-dichloropyridazin-3(2H)-ones without solvent at $100^\circ}C$. Aliphatic and aromatic alcohols were converted into the corresponding esters in good to excellent yields. It is noteworthy that the reaction is solvent-free, atom-economic, easy-workup, and rapid and that the process is inexpensive.
    原子经济性的酯化反应在绿色化学中极为重要。在本研究中,我们展示了在无溶剂条件下,通过醇与2-酰基-4,5-二氯哒嗪-3(2H)-酮反应,无需催化剂和添加剂,在$100^\circ}C$下实现醇的酯化反应。脂肪族和芳香族醇均能以良好至优异的产率转化为相应酯。值得注意的是,该反应无溶剂、原子经济性高、操作简便、反应迅速且成本低廉。
  • Eco-friendly atom-economical synthesis of 2-substituted-benzo[d]thiazoles and 2-substituted-benzo[d]oxazoles using 2-acylpyridazin-3(2H)-ones
    作者:Gi Hyeon Sung、In-Hye Lee、Bo Ram Kim、Dong-Soo Shin、Jeum-Jong Kim、Sang-Gyeong Lee、Yong-Jin Yoon
    DOI:10.1016/j.tet.2013.02.093
    日期:2013.4
    Efficient and green syntheses of heterocycles are of great importance. In this work, we have demonstrated the synthesis of benzo[d]thiazoles and benzo[d]oxazoles using 2-acylpyridazin-3(2H)-ones as acyl transfer agents under transition-metal-free and eco-friendly conditions. It is worthy to note that the reaction is efficient, green, and economical, and will find several applications in organic synthesis, medicinal chemistry, and industrial chemistry. (C) 2013 Elsevier Ltd. All rights reserved.
  • Catalyst-free esterification of alcohols using 2-acyl-4,5-dichloropyridazinones under microwave conditions
    作者:Bo Ram Kim、Gi Hyeon Sung、Sang-Gyeong Lee、Yong Jin Yoon
    DOI:10.1016/j.tet.2013.02.046
    日期:2013.4
    Efficient and green esterification is of great importance. In this work, we demonstrate the catalyst-free esterification of alcohols by their reaction with 2-acy1-4,5-dichloropyridazin-3(2H)-ones under microwave irradiation. Aliphatic and aromatic alcohols were converted into the corresponding esters in good to excellent yields under microwave irradiation in solvent or solvent-free conditions. It is noteworthy that the reaction is catalyst-free, atom-economic, and rapid and that the process is inexpensive. (C) 2013 Elsevier Ltd. All rights reserved.
  • Facile Esterification of Alcohols with 2-Acyl-4,5-dichloropyridazin-3(2H)-ones under Friedel–Crafts Conditions
    作者:Hyo Yoon、Yong-Jin Yoon、Bo Kim、Gi Sung、Ki Ryu、Sang-Gyeong Lee
    DOI:10.1055/s-0034-1378335
    日期:——
    This paper describes the esterification of aromatic and aliphatic alcohols by using 2-acyl-4,5-dichloropyridazin-3(2H)-ones as an acyl source under Friedel Crafts conditions. Twelve alcohols were reacted with four 2-acyl-4,5-dichloropyridazin-3(2H)-ones in the presence of AlCl3 in tetrahydrofuran at room temperature to give the corresponding esters in moderate to excellent yields. Thus, 2-acylpyridazin-3(2H)-ones serve as good and atom-economic acyl sources for the esterification of aromatic alcohols under Friedel Crafts conditions, representing a rapid, practical, and efficient method of esterification.
  • Carmellino; Massolini; Pagani, Il Farmaco, 1993, vol. 48, # 10, p. 1427 - 1438
    作者:Carmellino、Massolini、Pagani、Zani、Leri
    DOI:——
    日期:——
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