3-amino-9-methoxy-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one | 179024-59-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯二氮卓类
• 英文名称: 3-amino-9-methoxy-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one
• 英文别名: (3R)-3-Amino-9-methoxy-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one；(11R)-11-amino-6-methoxy-9-phenyl-1,10-diazatricyclo[6.4.1.04,13]trideca-4(13),5,7,9-tetraen-12-one
• CAS: 179024-59-0
• 化学式: C₁₈H₁₇N₃O₂
• 分子量: 307.352
• InChiKey: OXNJEXXVDKLIPL-QGZVFWFLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  23
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  67.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  异喹啉-3-甲酸 、 3-amino-9-methoxy-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one 在 O-[(ethoxycarbonyl)cyanomethyleneamino]-N,N,N',N'-tetramethyluronium tetrafluoroborate 、 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 (3R)-Isoquinoline-3-carboxylic acid (9-methoxy-4-oxo-1-phenyl-3,4,6,7-tetrahydro[1,4]diazepino-[6,7,1-hi]indol-3-yl)amide
  参考文献：
  名称：

  Synthesis and structure–activity relationships of 4-oxo-1-phenyl-3,4,6,7-tetrahydro-[1,4]diazepino[6,7,1- hi ]indoles: novel PDE4 inhibitors

  摘要：

  A novel series of benzodiazepine derivatives have been discovered as inhibitors of PDE4 enzymes. We have found that our compounds are selective versus other PDE enzymes, and that the activity can be modulated by specific structural modifications. One compound exhibited a strong eosinophilic infiltration inhibiting action on sensitized Brown-Norway rats (compound 9, 5.1 mg/kg p.o.), moreover this compound is not emetic at 3 mg/kg i.v. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(99)00573-9
• 作为产物：
  描述：

  5-甲氧基吲哚啉 在 Ru-carbon 吡啶 、 三氯化铝 、 potassium tert-butylate 、 氢气 、 三氯化硼 、 亚硝酸异戊酯 作用下， 以 四氢呋喃 、 甲醇 、 1,2-二氯乙烷 为溶剂， 生成 3-amino-9-methoxy-1-phenyl-6,7-dihydro-3H-[1,4]diazepino[6,7,1-hi]indol-4-one
  参考文献：
  名称：

  Synthesis and structure–activity relationships of 4-oxo-1-phenyl-3,4,6,7-tetrahydro-[1,4]diazepino[6,7,1- hi ]indoles: novel PDE4 inhibitors

  摘要：

  A novel series of benzodiazepine derivatives have been discovered as inhibitors of PDE4 enzymes. We have found that our compounds are selective versus other PDE enzymes, and that the activity can be modulated by specific structural modifications. One compound exhibited a strong eosinophilic infiltration inhibiting action on sensitized Brown-Norway rats (compound 9, 5.1 mg/kg p.o.), moreover this compound is not emetic at 3 mg/kg i.v. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(99)00573-9

文献信息

• Method for preparing substituted [1,4]diazepino[6,7,1-hi]indol-4-ones
  申请人：Warner-Lambert LLC

  公开号：US06689881B1

  公开（公告）日：2004-02-10

  Method for the preparation of enantiomerically pure diazepino-indolone of formula which comprises the intramolecular cyclization of a product of formula where A, B, X1, X2, Z, Z1, Z2 and R are as defined in the description, in the presence of a weak Lewis acid catalyst.

  一种制备对映纯的式子为的二氮杂环吲哚酮的方法，包括在弱Lewis酸催化剂存在下进行式子的分子内环化，其中式子中的A、B、X1、X2、Z、Z1、Z2和R的定义如说明书所述。
• [EN] DIAZEPINO-INDOLES AS PHOSPHODIESTERASE IV INHIBITORS<br/>[FR] DIAZEPINO-INDOLES INHIBITEURS DE PHOSPHODIESTERASES 4
  申请人：INSTITUT DE RECHERCHE JOUVEINAL

  公开号：WO1997036905A1

  公开（公告）日：1997-10-09

  (EN) Diazepino-indoles of formula (I), wherein A is mono- to trisubstituted aryl or heteroaryl, and B is an -OR1 or -NR2R3 group where R1, R2 and R3 are particularly hydrogen, and racemic forms, enantiomers and pharmaceutically acceptable salts thereof, as phosphodiesterase IV inhibitors, are disclosed.(FR) Diazépino-indoles de formule (I) dans laquelle A est aryle ou hétéroaryle mono- à trisubstitué, B est un groupe -OR1 ou -NR2R3, où R1, R2, R3 sont notamment hydrogènes, leurs formes racémiques, leurs énantiomères, et leurs sels pharmaceutiquement acceptables; qui sont inhibiteurs de phosphodiestérases 4.

  (I)式中，A为单取代至三取代芳基或杂环芳基，B为-OR1或-NR2R3基团，其中R1、R2和R3特别为氢，其外消旋体、对映体和药学上可接受的盐，作为磷酸二酯酶IV抑制剂。
• Diazépino-indoles inhibiteurs de phosphodiestérases 4
  申请人：INSTITUT DE RECHERCHE JOUVEINAL

  公开号：EP1132390A2

  公开（公告）日：2001-09-12

  Diazépino-indoles de formule (I) dans laquelle : A est aryle ou hétéroaryle mono- à trisubstitué, B est un groupe -OR1 ou -NR2R3, où R1, R2, R3 sont notamment hydrogènes, leurs formes racémiques, leurs énantiomères, et leurs sels pharmaceutiquement acceptables ; qui sont inhibiteurs de phosphodiestérases 4.

  式 (I) 的二氮杂吲哚 其中 ： A 是一至三取代的芳基或杂芳基、 B 是基团 -OR1 或 -NR2R3，其中 R1、R2 和 R3 尤其是氢、 它们的外消旋形式、它们的对映体以及它们的药学上可接受的盐； 是磷酸二酯酶 4 抑制剂。
• Synthesis, Structure−Activity Relationships, and Pharmacological Profile of 9-Amino-4-oxo-1-phenyl-3,4,6,7-tetrahydro[1,4]diazepino[6,7,1-<i>h</i><i>i</i>]indoles:  Discovery of Potent, Selective Phosphodiesterase Type 4 Inhibitors
  作者：Catherine Burnouf、Eric Auclair、Nadine Avenel、Bernadette Bertin、Christèle Bigot、Alain Calvet、Kam Chan、Corinne Durand、Veronique Fasquelle、Frédéric Féru、Richard Gilbertsen、Henry Jacobelli、Adel Kebsi、Emmanuelle Lallier、Jacquie Maignel、Brigitte Martin、Stéphane Milano、Malika Ouagued、Yves Pascal、Marie-Pierre Pruniaux、Jocelyne Puaud、Marie-Noëlle Rocher、Christophe Terrasse、Roger Wrigglesworth、Annette M. Doherty

  DOI：10.1021/jm000315p

  日期：2000.12.1

  The synthesis, structure-activity relationships, and biological properties of a novel series of; potent and selective phosphodiesterase type 4 (PDE4) inhibitors are described. These new aminodiazepinoindoles displayed in vitro PDE4 activity with submicromolar IC50 values and PDE4 selectivity vs PDE1, -3, and -5. Specifically, one compound (CI-1044, 10e) provided efficient in vitro inhibition of TNF alpha release from hPBMC and; hWB with IC50:values of 0.34 and 0.84 muM, respectively. This compound was found to exhibit potent in vivo activity in antigen-induced eosinophil recruitment in Brown-Norway rats (ED50 = 3.2 mg/kg po) and in production of TNF alpha in Wistar fats (ED50 = 2.8; mg/kg po). No emetic side effects at therapeutic doses were observed in ferrets.
• DIAZEPINO-INDOLES INHIBITEURS DE PHOSPHODIESTERASES IV
  申请人：INSTITUT DE RECHERCHE JOUVEINAL (I.R.J)

  公开号：EP0785789A1

  公开（公告）日：1997-07-30