3-o-Methoxyphenyl-4-methyl-1,2-dihydrochinolin-2-on | 70751-26-7

• 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: 3-o-Methoxyphenyl-4-methyl-1,2-dihydrochinolin-2-on
• 英文别名: 3-(2-methoxy-phenyl)-4-methyl-1H-quinolin-2-one；3-(2-methoxyphenyl)-4-methyl-1H-quinolin-2-one
• CAS: 70751-26-7
• 化学式: C₁₇H₁₅NO₂
• 分子量: 265.312
• InChiKey: XLCTUEHJYOEIQA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  38.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-o-Methoxyphenyl-4-methyl-1,2-dihydrochinolin-2-on 在 三氯氧磷 作用下， 反应 2.0h， 生成 2-Chloro-3-(2-methoxy-phenyl)-4-methyl-quinoline
  参考文献：
  名称：

  Synthesis and 5-hydroxytryptamine antagonist activity of 2-[[2-(dimethylamino)ethyl]thio]-3-phenylquinoline and its analogs

  摘要：

  A series of 2-[(2-aminoethyl)thio]quinolines substituted at the 3-position with alkyl, aryl, or heteroaryl groups has been prepared in the search for novel and selective 5-HT2 antagonists. The affinity of the compounds for 5-HT1 receptor sites was measured by their ability to displace [3H]-5-HT from rat brain synaptosomes whereas the affinity for 5-HT2 receptor sites was measured by their ability to displace [3H]spiperone from synaptosomes prepared from rat brain cortex. The 5-HT2 antagonist properties of the compounds were measured in vivo by their antagonism of 5-hydroxytryptophan-induced head twitches in the mouse and by their antagonism of hyperthermia induced by fenfluramine (N-ethyl-alpha-methyl-m-(trifluoromethyl)phenethylamine hydrochloride) in the rat. The structure-activity relationships in this series are discussed and the properties of 2-[[2-(dimethylamino)ethyl]thio]-3-phenylquinoline hydrochloride (70) are highlighted.

  DOI：

  10.1021/jm00395a013
• 作为产物：
  描述：

  N-(2-acetylphenyl)-2-(3-methoxyphenyl)acetamide 生成 3-o-Methoxyphenyl-4-methyl-1,2-dihydrochinolin-2-on
  参考文献：
  名称：

  BLACKBURN, THOMAS P.;COX, BARRY;GUILDFORD, ALLEN J.;LE, COUNT DAVID J.;MI+, J. MED. CHEM., 30,(1987) N 12, 2252-2259

  摘要：

  DOI：

文献信息

• The synthesis of benzofuroquinolines. I. Some benzofuro[2,3-<i>b</i>]quinoline and benzofuro[3,2-<i>c</i>]quinoline derivatives
  作者：Yoshiyuki Kawase、Seiji Yamaguchi、Osamu Maeda、Akemi Hayashi、Ichihiro Hayashi、Kazuko Tabata、Masako Kondo

  DOI：10.1002/jhet.5570160315

  日期：1979.4

  Benzofuro[2,3-b]quinoline (Ia) and its 11-methyl derivative (Ib) were synthesized by demethylcyclization of 3-(o-methoxyphenyl)-1,2-dihydroquinolin-2-ones (VIa,b). Benzofuro[2,3-b]quinoline-11-carboxylic acid (Id) was synthesized by chlorination followed by the action of potassium hydroxide of a lactone (IX) prepared by demethyl-cyclization of 3-(o-methoxyphenyl)-2-oxo-1,2-dihydroquinoline-4-carboxylic

  通过3-（邻甲氧基苯基）-1,2-二氢喹啉-2-酮（VIa，b）的脱甲基环化反应合成苯并呋喃[2,3- b ]喹啉（Ia）及其11-甲基衍生物（Ib）。苯并呋喃[2,3 - b ]喹啉-11-羧酸（Id）通过氯化反应，然后通过3-（邻甲氧基苯基）-2-的甲基环化反应制得的内酯（IX）的氢氧化钾作用合成氧代1,2-二氢喹啉-4-羧酸（VIII）。异构苯并呋喃[3,2-c]喹啉（Ha）及其6-甲基衍生物（IIb）是通过3-（o-甲氧基苯基）-1,4-二氢喹啉-4-酮（XIa，b）。通过与苯甲醛缩合，然后氧化，将两种甲基衍生物（Ib和IIb）都转化为羧酸（Id和IId）。由此获得的苯并呋喃喹啉（Ia，b，d和IIa，b）被氧化成相应的N-氧化物（IIIa，b，d和IVa，b）。
• KAWASE Y.; YAMAGUCHI S.; MAEDA O.; HAYASHI A.; HAYASHI I.; TABATA K.; KON+, J. HETEROCYCL. CHEM., 1979, 16, NO 3, 487-491
  作者：KAWASE Y.、 YAMAGUCHI S.、 MAEDA O.、 HAYASHI A.、 HAYASHI I.、 TABATA K.、 KON+

  DOI：——

  日期：——