6-(dipropylamino)-1,2,6,7-tetrahydro-3H,5H-pyrido<1,2,3-de>quinoxalin-3-one | 132874-90-9

• 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: 6-(dipropylamino)-1,2,6,7-tetrahydro-3H,5H-pyrido<1,2,3-de>quinoxalin-3-one
• 英文别名: 1,2,6,7-tetrahydro-6-(dipropylamino)-3H,5H-pyrido(1,2,3-de)quinoxalin-3-one；6-Dipropylamino-1,2,6,7-tetrahydro-5H-pyrido[1,2,3-de]quinoxalin-3-one；11-(dipropylamino)-1,4-diazatricyclo[7.3.1.05,13]trideca-5,7,9(13)-trien-2-one
• CAS: 132874-90-9
• 化学式: C₁₇H₂₅N₃O
• 分子量: 287.405
• InChiKey: AGDDFINMHZZBNF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  21
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  35.6
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  N-(1-formyl-1,2,3,4-tetrahydro-3-quinolyl)formamide 在 palladium on activated charcoal 盐酸 、 sodium nitrate 、 氢气 、 溴 、 sodium acetate 、 sodium carbonate 、 溶剂黄146 作用下， 以 四氢呋喃 、 乙醇 、 N,N-二甲基甲酰胺 、 三氟乙酸 为溶剂， 反应 46.5h， 生成 6-(dipropylamino)-1,2,6,7-tetrahydro-3H,5H-pyrido<1,2,3-de>quinoxalin-3-one
  参考文献：
  名称：

  Dopaminergic and serotonergic activities of imidazoquinolinones and related compounds

  摘要：

  The synthesis of 5-(dipropylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (5), a potent dopamine D2 agonist showing high dopamine/serotonin (5HT1A) selectivity, is described. Dopaminergic activity is associated with the (R)-enantiomer of 5; the (S)-enantiomer shows no dopaminergic activity. A series of analogues where the imidazolone ring was modified to various 5- or 6-membered heterocyclic rings were prepared. Some of these compounds showed a combination of dopaminergic and serotonergic activity, while one compound, 6-(dipropylamino)-1,2,6,7-tetrahydro-3H,5H-pyrido[3,2,1-ij]quinazolin-3-one (24), was a selective serotonergic agonist. Various analogues of 5 where the dipropylamine substituent was modified were prepared. Most of these showed reduced dopaminergic activity, while several were as potent as 5 at the serotonin 5HT1A receptor. Orientations for the new compounds at dopamine and serotonin receptors are proposed and compared with those of other tricyclic ligands known to have high affinity at these receptors.

  DOI：

  10.1021/jm00084a013

文献信息

• ANTITUSSIVE
  申请人：TORAY INDUSTRIES, INC.

  公开号：EP0636371A1

  公开（公告）日：1995-02-01

  An antitussive containing a δ-opioid antagonist or a pharmacologically acceptable salt thereof as the active ingredient. It has a potent activity, does not give side effects such as impaired mentation, and can be administered perorally.

  一种含有δ-类阿片拮抗剂或其药理上可接受的盐作为活性成分的止咳药。它具有很强的活性，不会产生副作用（如精神受损），并且可以经口给药。
• HETEROCYCLIC AMINES HAVING CENTRAL NERVOUS SYSTEM ACTIVITY
  申请人：THE UPJOHN COMPANY

  公开号：EP0480939B1

  公开（公告）日：1995-01-25
• US5273975A
  申请人：——

  公开号：US5273975A

  公开（公告）日：1993-12-28
• US5436240A
  申请人：——

  公开号：US5436240A

  公开（公告）日：1995-07-25
• [EN] HETEROCYCLIC AMINES HAVING CENTRAL NERVOUS SYSTEM ACTIVITY
  申请人：THE UPJOHN COMPANY

  公开号：WO1990015058A1

  公开（公告）日：1990-12-13

  (EN) Tricyclic nitrogen containing compounds, having central nervous system activity of structural formula (I) and pharmaceutically acceptable salts thereof, wherein R1, R2, and R3 are independently hydrogen, C1-6 alkyl, alkenyl, or alkynyl, C3-10 cycloalkyl, or R1 and R2 are joined to form a C3-7 cyclic amine which can contain additional heteroatoms; X is hydrogen, C1-6 alkyl, halogen, hydroxy, alkoxy, cyano, carboxamide, carboxyl, or carboalkoxyl; A is SO2, N, CH, CH2, CHCH3, C=O, C=S, C-SCH3, C=NH, C-NH2, C-NHCH3, C-NHCOOCH3, or C-NHCN; B is CH2, CH, C=O, N, NH or N-CH3; n is 0 or 1; and D is CH, CH2, C=O, O, N, NH or N-CH3. These new compounds are suitable for treating schizophrenia, Parkinson's disease, anxiety, depression or as compounds for lowering blood pressure in animal or human hosts.(FR) De l'azote tricyclique comprenant des composés agissant sur le système nerveux central et correspondant à la formule de structure (I), et leur sels acceptables en pharmaceutique, où R1, R2 et R3 sont indépendamment l'hydrogène, un alkyle C1-6, un alkényle, ou un alkynyle, un cycloalkyle C3-10, ou bien R1 et R2 sont liés et forment une amine cyclique C3-7 qui peut contenir des hétéroatomes supplémentaires; X est l'hydrogène, un alkyle C1-6, l'halogène, l'hydroxy, l'alkoxy, le cyano, le carboxamide, le carboxyle, ou carboalkoxyle; A est SO2, N, CH, CH2, CHCH3, C=O, C=S, C-SCH3, C=NH, C-NH2, C-NHCH3, C-NHCOOCH3, ou C-NHCN; B est CH2, CH, C=O, N, NH, ou N-CH3; n est 0 ou 1; et D est CH, CH2, C=O, O, N, NH ou N-CH3. Lesdits composés sont utilisables dans le traitement de la schizophrénie, de la maladie de Parkinson, de l'anxiété, de la dépression ou, en tant que composés, pour abaisser la tension artérielle dans des hôtes humains ou animaux.