(4-氯苯基)-喹唑啉-4-基甲酮 | 55276-59-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: (4-氯苯基)-喹唑啉-4-基甲酮
• 英文名称: (4-chloro-phenyl)-quinazolin-4-yl-methanone
• 英文别名: Methanone, (4-chlorophenyl)-4-quinazolinyl-；(4-chlorophenyl)-quinazolin-4-ylmethanone
• CAS: 55276-59-0
• 化学式: C₁₅H₉ClN₂O
• 分子量: 268.702
• InChiKey: JTAYRFYLCGTNNG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  42.8
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (4-氯苯基)-喹唑啉-4-基甲酮 在 氢氧化钾 、 sodium hydroxide 、 potassium hexacyanoferrate(III) 作用下， 以 水 、 二甲基亚砜 、 苯 为溶剂， 反应 2.0h， 生成 4-(4-chlorophenyl)quinazoline
  参考文献：
  名称：

  Higashino, Takeo; Takemoto, Masumi; Hayashi, Eisaku, Chemical and pharmaceutical bulletin, 1985, vol. 33, # 4, p. 1351 - 1359

  摘要：

  DOI：
• 作为产物：
  描述：

  3-benzoyl-3,4-dihydro-4-quinazolinecarbonitrile 在 sodium hydroxide 、 sodium hydride 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 0.5h， 生成 (4-氯苯基)-喹唑啉-4-基甲酮
  参考文献：
  名称：

  Higashino, Takeo; Takemoto, Masumi; Hayashi, Eisaku, Chemical and pharmaceutical bulletin, 1985, vol. 33, # 4, p. 1351 - 1359

  摘要：

  DOI：

文献信息

• Carbon-Carbon Bond Cleavage of .ALPHA.-Hydroxybenzylheteroarenes Catalyzed by Cyanide Ion: Retro-Benzoin Condensation Affords Ketones and Heteroarenes and Benzyl Migration Affords Benzylheteroarenes and Arenecarbaldehydes.
  作者：Yumiko SUZUKI、Yuki TAKEMURA、Ken-ichi IWAMOTO、Takeo HIGASHINO、AKira MIYASHITA

  DOI：10.1248/cpb.46.199

  日期：——

  4-(α-Benzyl-α-hydroxybenzyl)quinazoline (4a) underwent retro-benzoin condensation catalyzed by cyanide ion to give deoxybenzoin (2a) and quinazoline (5a). Similarly, several nitrogen-containing heteroarenes (4, 9, 12, 16-19) having an α-hydroxybenzyl group at the α-position of the nitrogen underwent retro-benzoin type condensation to afford ketones (2) and heteroarenes (5). However, similar reaction of pyrazolopyrimidines (13, 14, 15) having an α-benzyl-α-hydroxybenzyl group resulted in benzyl migration, giving benzylpyrazolopyrimidines (8) and arenecarbaldehydes (3). Tetrabutylammonium cyanide (11, Bu4NCN) was a more effective cyanide ion donor than KCN (10). The retro-benzoin condensation was applied to the synthesis of 2-substituted quinazolines (38) from 2-chloro-4-aroylquinazolines (34), using the aroyl group as a protecting and electron-withdrawing group.

  4-(α-苄基-α-羟基苄基)喹唑啉(4a)在氰离子催化下经历逆苯偶姻缩合反应，生成脱氧苯偶姻(2a)和喹唑啉(5a)。同样，多个含氮杂环芳烃(4, 9, 12, 16-19)在其氮原子的α位上具有α-羟基苄基的结构，也经历逆苯偶姻型缩合反应，生成了酮(2)和杂环芳烃(5)。然而，具有α-苄基-α-羟基苄基结构的吡唑嘧啶(13, 14, 15)在类似的反应中引发了苄基迁移，生成了苄基吡唑嘧啶(8)和芳烃羰醛(3)。四丁基铵氰(11, Bu4NCN)比KCN(10)更有效地作为氰离子的供体。逆苯偶姻缩合反应被应用于从2-氯-4-芳酰基喹唑啉(34)合成2-取代喹唑啉(38)，使用芳酰基作为保护和电子 withdrawing 基团。
• Catalytic Action of Azolium Salts. II. Aroylation of 4-Chloroquinazolines with Aromatic Aldehydes Catalyzed by 1,3-Dimethylbenzimidazolium Iodide.
  作者：Akira MIYASHITA、Hideaki MATSUDA、Chihoko IIJIMA、Takeo HIGASHINO

  DOI：10.1248/cpb.40.43

  日期：——

  When a mixture of 4-chloroquinazoline (7), an aromatic aldehyde 6, sodium hydride, and a catalytic amount of 1, 3-dimethylbenzimidazolium iodide (1) in tetrahydrofuran (THF) was refluxed with stirring for an appropriate time, the chlorine atom of 7 was replaced with the aroyl group, and the 4-aroylquinazolines 10 were obtained in excellent yields. Similar treatments of 4-chloro-2-methylquinazoline (8) and 4-chloro-2-phenylquinazoline (9) led to the 4-aroyl-2-methylquinazolines 11 and the 4-aroyl-2-phenylquinazolines 12, respectively.Use of N, N-dimethylformamide (DMF) instead of THF as the reaction solvent in the above reaction reduced the reaction time and increased the yields of the ketones 10 and 12 as compared with those in THF.

  当4-氯喹唑啉（7）、芳香醛6、氢化钠和催化量的1,3-二甲基苯并咪唑碘化物（1）在四氢呋喃（THF）中搅拌回流适当时间后，7中的氯原子被芳酰基取代，得到产率极佳的4-芳酰基喹唑啉10。类似地处理4-氯-2-甲基喹唑啉（8）和4-氯-2-苯基喹唑啉（9），分别得到4-芳酰基-2-甲基喹唑啉11和4-芳酰基-2-苯基喹唑啉12。在上述反应中使用N,N-二甲基甲酰胺（DMF）而非THF作为反应溶剂，相比THF，可以缩短反应时间并提高酮10和12的产率。
• Synthesis and Structure–Activity Relationship Study of 1-Phenyl-1-(quinazolin-4-yl)ethanols as Anticancer Agents
  作者：Kenta Kuroiwa、Hirosuke Ishii、Kenji Matsuno、Akira Asai、Yumiko Suzuki

  DOI：10.1021/ml5004684

  日期：2015.3.12

  NCI-H460 (lung), HCT116 (colon), MCF7 (breast), PC3 (prostate), and HeLa (cervical) cells with IC50 values from 0.1 to 0.3 muM. A structure-activity relationship (SAR) study at the 2- and 4-position of the quinazoline core lead to the discovery of more potent anticancer agents (14, 16, 17, 19, 24, and 31). The results of an in vitro tubulin polymerization assay and fluorescent-based colchicine site competition

  喹唑啉衍生物PVHD121（1a）已显示出对多种肿瘤衍生细胞系（包括A549（肺），NCI-H460（肺），HCT116（结肠），MCF7（乳腺），PC3（前列腺），和HeLa（子宫颈）细胞，IC50值为0.1至0.3μM。在喹唑啉核心的2位和4位进行的结构活性关系（SAR）研究导致发现了更有效的抗癌药（14、16、17、19、24和31）。体外微管蛋白聚合测定和纯化的微管蛋白的基于荧光的秋水仙碱位点竞争测定的结果表明1a通过与秋水仙碱位点结合来抑制微管蛋白聚合。
• Catalytic Action of Azolium Salts. IV. Preparations of 4-Aroylquinazolines and 4-Aroyl-1H-pyrazolo(3,4-d)pyrimidines by Catalytic Action of 1,3-Dimethylimidazolium Iodide.
  作者：Akira MIYASHITA、Hideaki MATSUDA、Yumiko SUZUKI、Ken-ichi IWAMOTO、Takeo HIGASHINO

  DOI：10.1248/cpb.42.2017

  日期：——

  The ability of 1, 3-dimethylimidazolium iodide (1) to catalyze the aroylation of the chloroheteroarenes 4-8 with arenecarbaldehydes 3 as sources of the aroyl groups was examined in order to develop a preparative method of aroylheteroarenes. In the presence of 1, the treatment of the 4-chloroquinazolines (4 : 2-H, 5 : 2-Me, 6 : 2-Ph) with arenecarbaldehyde 3 in refluxing THF (tetrahydrofuran) or dioxane led to the 4-aroylquinazolines (9 : 2-H, 10 : 2-Me, 11 : 2-Ph) in excellent yields, as had been found with 1, 3-dimethylbenzimidazolium iodide (2). Similar reaction of the 4-chloro-1H-pyrazolo[3, 4-d]pyrimidines (7 : 1-Ph, 8 : 1-Me) with arenecarbaldehyde 3 yielded the corresponding 4-aroyl-1H-pyrazolo[3, 4-d]pyrimidines (12 : 1-Ph, 13 : 1-Me). Compound 1 seems to catalyze the aroylation of a wider range of arenecarbaldehydes 3 as compared with 2.

  研究了1,3-二甲基咪唑锭碘化物（1）催化氯杂芳烃4-8与芳烯羰基化合物3的芳酰基化反应的能力，以开发一种合成芳酰杂芳烃的新方法。在存在1的条件下，4-氯喹唑啉（4：2-H，5：2-Me，6：2-Ph）与芳烯羰基化合物3在回流的THF（四氢呋喃）或二噁烷中反应，得到了优良产率的4-芳酰喹唑啉（9：2-H，10：2-Me，11：2-Ph），这与1,3-二甲基苯并咪唑锭碘化物（2）得到的结果一致。类似地，4-氯-1H-吡唑[3,4-d]嘧啶（7：1-Ph，8：1-Me）与芳烯羰基化合物3反应，得到了相应的4-芳酰-1H-吡唑[3,4-d]嘧啶（12：1-Ph，13：1-Me）。与2相比，化合物1似乎能催化更广泛的芳烯羰基化合物3的芳酰基化反应。
• Transition metal-free regioselective direct acylation of quinazolines for the synthesis of acylquinazoline derivatives
  作者：Wei Chen、Jingjun Fang、Jian Huang、Qin Yang、Zhibin Song、Qiuping Ding、Hongming Wang、Yiyuan Peng

  DOI：10.1039/d3ob01349a

  日期：——

  An efficient, mild method for direct regioselective acylation of quinazolines under metal-free conditions was developed with bis(trifluoroacetoxy)iodobenzene and trimethylsilyl azide at ambient temperature. The acylation reaction of quinazolines with aldehydes gave the corresponding acyl quinazolines in ethyl acetate with good to excellent yields and excellent functional group tolerance and site selectivity

  开发了一种在无金属条件下用双（三氟乙酰氧基）碘苯和三甲基叠氮化物在环境温度下直接区域选择性酰化喹唑啉的高效、温和的方法。喹唑啉与醛的酰化反应在乙酸乙酯中产生相应的酰基喹唑啉，具有良好至优异的产率以及优异的官能团耐受性和位点选择性。此外，通过HPLC-HRMS（高压液相色谱-高分辨率质谱）和EPR（电子顺磁共振）策略研究了喹唑啉酮直接酰化的机理。