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3-(benzo[d]thiazol-2-yl)-2-phenyl-2,3-dihydroquinazolin-4(1H)-one | 1097967-82-2

中文名称
——
中文别名
——
英文名称
3-(benzo[d]thiazol-2-yl)-2-phenyl-2,3-dihydroquinazolin-4(1H)-one
英文别名
3-(2'-benzothiazolyl)-2,3-dihydro-2-(phenyl)-quinazolin-4(1H)-one;3-benzothiazol-2-yl-2-phenyl-2,3-dihydro-1H-quinazolin-4-one;3-(1,3-Benzothiazol-2-yl)-2-phenyl-1,2-dihydroquinazolin-4-one;3-(1,3-benzothiazol-2-yl)-2-phenyl-1,2-dihydroquinazolin-4-one
3-(benzo[d]thiazol-2-yl)-2-phenyl-2,3-dihydroquinazolin-4(1H)-one化学式
CAS
1097967-82-2
化学式
C21H15N3OS
mdl
——
分子量
357.436
InChiKey
QDQNKRNMZSAKQD-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):
    5.1
  • 重原子数:
    26
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    73.5
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    2-氨基苯并噻唑靛红酸酐苯甲醛 反应 2.2h, 以66%的产率得到3-(benzo[d]thiazol-2-yl)-2-phenyl-2,3-dihydroquinazolin-4(1H)-one
    参考文献:
    名称:
    在无溶剂和无催化剂条件下合成新型的3-(2'-苯并噻唑基)-2,3-二氢喹唑啉-4(1 H)-一
    摘要:
    开发了一种无溶剂和无催化剂的一锅式三组分缩合反应方法,用于在相对较快的范围内合成新型的3-(2'-苯并噻唑基)-2,3-二氢喹唑啉-4(1 H)-酮。良品率高。
    DOI:
    10.1002/jhet.5570450612
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文献信息

  • Microwave-promoted one-pot three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones catalyzed by heteropolyanion-based ionic liquids under solvent-free conditions
    作者:Yang Yang、Renzhong Fu、Yang Liu、Jing Cai、Xiaojun Zeng
    DOI:10.1016/j.tet.2020.131312
    日期:2020.7
    3-dihydroquinazoline-4(1H)-one derivatives have been synthesized via one-pot three-component reaction using isatoic anhydrides, amines and aldehydes (or ketones) catalyzed by heteropolyanion-based ionic liquids under microwave-promoted conditions. The practical protocol was found to tolerate a wide range of substrates with different functional groups. Moderate to excellent yields, solvent-free media and operational
    在微波促进下,通过杂多阴离子基离子液体催化的等位酸酐,胺和醛(或酮)通过一锅三组分反应合成了一系列2,3-二氢喹唑啉-4(1 H)-one衍生物。条件。发现该实用方案可耐受具有不同官能团的多种底物。中等至极好的产量,无溶剂介质和操作简便是主要亮点。此外,催化剂可以回收和再利用而没有明显的反应性损失。与现有方法相比,该方法提供了绿色且经过改进的协议。
  • One-pot synthesis of 1-(benzothiazolylamino)aryl methyl-2-naphthols and 3-benzothiazolyl 2,3-dihydroquinazolinones using a magnetically recoverable core–shell nanocomposite as catalyst
    作者:Yousef Mardani、Zahed Karimi-Jaberi、Mohammad Jaafar Soltanian Fard
    DOI:10.1515/znb-2021-0010
    日期:——
    Abstract

    Nano-magnetite-supported sulfated polyethylene glycol (Fe3O4@PEG-SO3H) was prepared, characterized and utilized as a magnetically recoverable heterogeneous catalyst for the one-pot, three-component reaction of 2-aminobenzothiazole, aldehydes and 2-naphthol/isatoic anhydride resulting in efficient formation of 1-(benzothiazolylamino)arylmethyl-2-naphthol or dihydroquinazolinones derivatives. The significant features of this method include green conditions, operational simplicity, minimizing production of chemical waste, shorter reaction times and good to high yields. In addition, the nanocatalyst can easily be separated from the reaction mixture by application of a magnetic field and reused without significant deterioration in its catalytic activity.

    标题:摘要 纳米磁矿物负载磺酸乙二醇Fe3O4@PEG-SO3H)已经制备、表征并用作可磁回收的异相催化剂,用于2-氨基苯并噻唑醛类2-萘酚/异安酸酐的一锅法三组分反应,从而高效形成1-(苯并噻唑基)芳基甲基-2-萘酚或二氢喹唑啉生物。该方法的显著特点包括绿色条件、操作简便、最小化化学废物的产生、较短的反应时间和良好至高产率。此外,纳米催化剂可以通过施加磁场轻松地从反应混合物中分离出来,并在不显著降低其催化活性的情况下进行重复使用。
  • Synthesis, characterization and catalytic application of tributyl(carboxymethyl)phosphonium bromotrichloroferrate as a new magnetic ionic liquid for the preparation of 2,3-dihydroquinazolin-4(1H)-ones and 4H-pyrimidobenzothiazoles
    作者:Mohammad Reza Anizadeh、Mohammad Ali Zolfigol、Meysam Yarie、Morteza Torabi、Saeid Azizian
    DOI:10.1007/s11164-020-04183-y
    日期:2020.8
    magnetic ionic liquid bearing acetic acid tags was synthesized and characterized by several methods including Fourier transform infrared spectroscopy (FT-IR), energy-dispersive X-ray spectroscopy (EDX), vibrating sample magnetometer (VSM), thermogravimetric analysis (TGA) and derivative thermogravimetry analysis (DTG). The prepared magnetic ionic liquid was applied as catalyst for synthesis of 2,3-
    摘要 本文合成了带有乙酸标签的新型三丁基(羧甲基)酸fer盐,并通过傅里叶变换红外光谱(FT-IR),能量色散X射线光谱(EDX),振动等方法进行了表征。样品磁力计(VSM),热重分析(TGA)和微分热重分析(DTG)。将所制备的磁性离子液体用作在无溶剂条件下合成2,3-二氢喹唑啉-4(1 H)-ones和4 H-嘧啶苯并噻唑生物的催化剂。 图形摘要 新型磁性离子液体对合成2,3-二氢喹唑啉-4(1 H)-ones和4 H-嘧啶苯并噻唑生物具有很高的催化性能。
  • New applications of phosphoric acid supported on alumina (H3PO4–Al2O3) as a reusable heterogeneous catalyst for preparation of 2,3-dihydroquinazoline-4(1H)-ones, 2H-indazolo[2,1-b]phthalazinetriones, and benzo[4,5]imidazo[1,2-a]pyrimidines
    作者:Hamid Reza Shaterian、Nafiseh Fahimi、Kobra Azizi
    DOI:10.1007/s11164-013-1087-2
    日期:2014.5
    An eco-friendly procedure for synthesis of 2,3-dihydroquinazoline-4(1H)-one, 2H-indazolo[2,1-b]phthalazinetrione, and benzo[4,5]imidazo[1,2-a]pyrimidine derivatives by three-component reaction, with phosphoric acid supported on alumina as catalyst, is described. Noticeable features of the method are that it is solvent-free, work-up is easy, yields are excellent, and the catalyst is reusable.
    合成2,3-二氢喹唑啉-4(1 H)-one,2 H-吲唑并[ 2,1 - b ]邻苯二氮杂三酮和苯并[4,5]咪唑并[1,2- a ]的环保方法描述了三组分反应的嘧啶生物,其中磷酸负载在氧化铝上作为催化剂。该方法的显着特征是无溶剂,后处理容易,产率极好并且催化剂可重复使用。
  • Agar: a novel, efficient, and biodegradable catalyst for the one-pot three-component and green synthesis of 2,3-dihydroquinazolin-4(1H)-one, 4H-pyrimidobenzothiazole and 2-aminobenzothiazolomethylnaphthol derivatives
    作者:Ashraf Moradi、Reza Heydari、Malek Taher Maghsoodlou
    DOI:10.1007/s11164-014-1818-z
    日期:2015.10
    Abstract 3-(2′-Benzothiazolyl)-2,3-dihydroquinazolin-4(1 H )- one, 1-((benzo[d]thiazol-2-ylamino) (aryl)-methyl)naphthalen-2-ol and 4 H -pyrimido[2,1-b][1,3]benzothiazoles derivatives were prepared via one-pot three-component reaction of arylaldehydes, 2-aminobenzothiazole and isatoic anhydride or β -naphthol or ethyl/methyl acetoacetate in the presence of agar as a highly efficient homogenous catalyst
    摘要 3-(2'-苯并噻唑基)-2,3-二氢喹唑啉-4(1 H )-一,1-((苯并[d]噻唑-2-基基)(芳基)-甲基)-2-醇和在芳烃存在下,通过芳醛,2-氨基苯并噻唑异丁酸酐或 β- 萘酚或乙基/甲基乙酰乙酸的一锅三组分反应制得4 H- 嘧啶并[2,1-b] [1,3]苯并噻唑生物 琼脂作为高效均质催化剂。使用无毒且可生物降解的催化剂以及高收率,较短的反应时间,简单的后处理和绿色条件是该方法的最重要优点。图形概要
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