2-acetoxy-2,5-dimethyl-2,3-dihydrofuro[3,2-c]quinolin-4(5H)-one | 128056-35-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 2-acetoxy-2,5-dimethyl-2,3-dihydrofuro[3,2-c]quinolin-4(5H)-one
• 英文别名: (2,5-dimethyl-4-oxo-3H-furo[3,2-c]quinolin-2-yl) acetate
• CAS: 128056-35-9
• 化学式: C₁₅H₁₅NO₄
• 分子量: 273.288
• InChiKey: WIPADMZNGDLCLO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  55.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  4-羟基-N-甲基-2-喹啉 在 碘 、 mercury(II) oxide 作用下， 以 甲醇 、 苯 为溶剂， 反应 8.0h， 生成 2-acetoxy-2,5-dimethyl-2,3-dihydrofuro[3,2-c]quinolin-4(5H)-one
  参考文献：
  名称：

  Photoinduced molecular transformations. 110. Formation of furoquinolinones via .beta.-scission of cyclobutanoxyl radicals generated from [2 + 2] photoadducts of 4-hydroxy-2-quinolone and acyclic and cyclic alkenes. X-ray crystal structure of (6a.alpha.,6b.beta.,10a.beta.,10b.alpha.)-(.+-.)-10b-acetoxy-6a,6b,7,8,9,10,10a,10b-octahydro-5-methylbenzo[3,4]cyclobuta[1,2-c]quinolin-6(5H)-one

  摘要：

  DOI：

  10.1021/jo00303a034

文献信息

• CAN-mediated Formation of Furopyranones and Furoquinolinones
  作者：Kazuhiro Kobayashi、Kouji Sakashita、Hideki Akamatsu、Koujirou Tanaka、Masaharu Uchida、Tomokazu Uneda、Taichi Kitamura、Osamu Morikawa、Hisatoshi Konishi

  DOI：10.3987/com-99-8688

  日期：——

  The reaction of 4-hydroxy-2H-pyran-2-one derivatives (1), (11), and (17) with a range of alkenes or phenylacetylene in acetonitrile containing cerium(IV) ammonium nitrate (CAN) afforded the corresponding furo[3,2-c]pyranone (4, 8, 13, 15, and 18) and/or furo[2,3-b]pyranone derivatives (6, 10, 14, 16, and 19). Similar treatment of 4-hydroxy-1-methylquinolin-2(1H)-one (2) with alkenes or phenylacetylene in the presence of CAN gave furo[3,2-c]quinolin-4(5H)-one derivatives (5) and (9).
• SUGINOME, HIROSHI;KOBAYASHI, KAZUHIRO;ITOH, MASAHITO;SEKO, SHINZO;FURUSAK+, J. ORG. CHEM., 55,(1990) N6, C. 4933-4943
  作者：SUGINOME, HIROSHI、KOBAYASHI, KAZUHIRO、ITOH, MASAHITO、SEKO, SHINZO、FURUSAK+

  DOI：——

  日期：——
• Photoinduced molecular transformations. 110. Formation of furoquinolinones via .beta.-scission of cyclobutanoxyl radicals generated from [2 + 2] photoadducts of 4-hydroxy-2-quinolone and acyclic and cyclic alkenes. X-ray crystal structure of (6a.alpha.,6b.beta.,10a.beta.,10b.alpha.)-(.+-.)-10b-acetoxy-6a,6b,7,8,9,10,10a,10b-octahydro-5-methylbenzo[3,4]cyclobuta[1,2-c]quinolin-6(5H)-one
  作者：Hiroshi Suginome、Kazuhiro Kobayashi、Masahito Itoh、Shinzo Seko、Akio Furusaki

  DOI：10.1021/jo00303a034

  日期：1990.8