4-[(6,7-二氢-5H-环五嘧啶-4-基)氨基]苯甲腈 | 786700-82-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 中文名称: 4-[(6,7-二氢-5H-环五嘧啶-4-基)氨基]苯甲腈
• 英文名称: 4-((2-methyl-4-(methyloxy)phenyl)amino)butanenitrile
• 英文别名: 4-[(4-Methoxy-2-methylphenyl)amino]butanenitrile；4-(4-methoxy-2-methylanilino)butanenitrile
• CAS: 786700-82-1
• 化学式: C₁₂H₁₆N₂O
• 分子量: 204.272
• InChiKey: CWTJEPCWJTZCIP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  15
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  45
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-[(6,7-二氢-5H-环五嘧啶-4-基)氨基]苯甲腈 在 盐酸 、 potassium tert-butylate 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 23.33h， 生成 6-methyl-1-[2-methyl-4-(methyloxy)phenyl]-1,2,3,7-tetrahydro-4H-pyrrolo[2,3-b]pyridin-4-one
  参考文献：
  名称：

  WO2006/108689

  摘要：

  公开号：
• 作为产物：
  描述：

  2-甲基-4-甲氧基苯胺 反应 6.0h， 以65%的产率得到4-[(6,7-二氢-5H-环五嘧啶-4-基)氨基]苯甲腈
  参考文献：
  名称：

  WO2006/108689

  摘要：

  公开号：

文献信息

• Identification of a Manufacturing Route of Novel CRF-1 Antagonists Containing a 2,3-Dihydro-1<i>H</i>-pyrrolo[2,3-<i>b</i>]pyridine Moiety
  作者：Arianna Ribecai、Sergio Bacchi、Monica Delpogetto、Simone Guelfi、Angelo Maria Manzo、Alcide Perboni、Paolo Stabile、Pieter Westerduin、Marie Hourdin、Sara Rossi、Stefano Provera、Lucilla Turco

  DOI：10.1021/op100147h

  日期：2010.7.16

  A case study on the synthesis of novel CRF-1 antagonists containing the 2,3-dihydro-1H-pyrrolo[2,3-b]pyridine moiety is presented. The development of ever more efficient synthetic routes allowed the progression of three candidates at the same time. A manufacturing route was identified and successfully demonstrated on a pilot-plant scale to prepare 100 kg of the CRF-1 antagonist GW876008.

  案例研究合成新型的CRF-1拮抗剂，其中包含2,3-二氢-1 H-吡咯并[2,3- b ]吡啶部分。越来越有效的合成路线的发展使三个候选物同时发展。确定了一条生产路线，并在中试规模上成功展示了制备100千克CRF-1拮抗剂GW876008的方法。
• PROCESS FOR PREPARING BICYCLIC COMPOUNDS
  申请人：Andreotti Daniele

  公开号：US20090023757A1

  公开（公告）日：2009-01-22

  The present invention relates to a novel process for preparing compounds of formula (IA), which are potent and specific antagonists of corticotropin-releasing factor (CRF) receptors, from intermediate compounds of formula (I), by a coupling reaction catalysed by copper.

  本发明涉及一种新型制备公式（IA）化合物的方法，该化合物是促肾上腺皮质激素释放因子（CRF）受体的强效特异性拮抗剂，该方法从公式（I）的中间体化合物出发，经过铜催化的偶联反应制备而成。
• Condensed n-heterocyclic compounds and their use as crf receptor antagonists
  申请人：Andreotti Daniele

  公开号：US20070004708A1

  公开（公告）日：2007-01-04

  The present invention provides compounds of formula (I) including stereoisomers, prodrugs and pharmaceutically acceptable salts or solvates thereof (Formula (I)) wherein the dashed line may represent a double bond; R is aryl or heteroaryl, each of which may be substituted by 1 to 4 groups J selected from: halogen, C1-C6 alkyl, C1-C6 alkoxy, halo C1-C6 alkyl, C2-C6 lkenyl, C2-C6 alkynyl, halo C1-C6 alkoxy, —C(O)R 2 , nitro, hydroxy, —NR 3 R 4 , cyano and or a group Z; R 1 is hydrogen, C3-C7 cycloalkyl, C1-C6 alkyl, C1-C6 alkoxy, C1-C6 thioalkyl, C2-C6 alkenyl, C2-C6 alkynyl, halo C1-C6 alkyl, halo C1-C6 alkoxy, halogen, NR 3 R 4 or cyano; D, G is —C— optionally substituted; X is carbon or nitrogen; Y is nitrogen or —C— optionally substituted; W is a 4-8 membered ring, which may be saturated or may contain one to three double bonds, and in which:—one carbon atom is replaced by a carbonyl or S(O) m ; and—one to four carbon atoms may optionally be replaced by oxygen, nitrogen or NR 12 , S(O) m , carbonyl, and such ring may be further substituted by 1 to 8 substituents; Z is a 5-6 membered heterocycle, which may be substituted by 1 to 8 R 5 groups or a phenyl ring, which may be substituted by 1 to 4 substituents; m is an integer from 0 to 2. to processes for their preparation, to pharmaceutical compositions containing them and to their use in the treatment of conditions mediated by corticotropin-releasing factor (CRF).

  本发明提供了式(I)的化合物，包括立体异构体、前药和其药学上可接受的盐或溶剂合物（式(I)），其中虚线可表示双键；R为芳基或杂环芳基，每个都可以被1到4个J基团替代，所述J基团选自：卤素、C1-C6烷基、C1-C6烷氧基、卤代C1-C6烷基、C2-C6烯基、C2-C6炔基、卤代C1-C6烷氧基、—C(O)R2、硝基、羟基、—NR3R4、氰基或Z基；R1为氢、C3-C7环烷基、C1-C6烷基、C1-C6烷氧基、C1-C6硫代烷基、C2-C6烯基、C2-C6炔基、卤代C1-C6烷基、卤代C1-C6烷氧基、卤素、NR3R4或氰基；D、G为可选取代的—C—；X为碳或氮；Y为氮或可选取代的—C—；W为4-8个成员的环，可以饱和或含有1-3个双键，在其中：—一个碳原子被羰基或S（O）m所取代；—1-4个碳原子可以被氧、氮或NR12、S（O）m、羰基所取代，并且该环可以进一步被1-8个取代基所取代；Z为5-6个成员的杂环，可以被1-8个R5基团或苯环所取代，该苯环可以被1-4个取代基所取代；m为0-2的整数。本发明还提供了制备这些化合物的方法，以及含有它们的药物组合物，并用于治疗由促肾上腺皮质激素释放因子（CRF）介导的疾病。
• Process for Preparing Bicyclic Compounds
  申请人：Bacchi Sergio

  公开号：US20080312444A1

  公开（公告）日：2008-12-18

  The present invention relates to a novel process for preparing compounds of formula (IA), which are potent and specific antagonists of corticotropin-releasing factor (CRF) receptors, from intermediate compounds of formula (I), by a coupling reaction catalysed by copper.

  本发明涉及一种新型制备式（IA）化合物的方法，该化合物是促肾上腺皮质激素释放因子（CRF）受体的有效和特异性拮抗剂，该方法通过铜催化的偶联反应从式（I）的中间体化合物制备得到。
• Condensed N-Heterocyclic Compounds and their Use as CRF Receptor Antagonists
  申请人：Andreotti Daniele

  公开号：US20110172255A1

  公开（公告）日：2011-07-14

  The present invention provides compounds of formula (I), processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of conditions mediated by corticotropin-releasing factor (CRF).

  本发明提供了式（I）的化合物，以及制备它们的方法，包含它们的制药组合物和它们在治疗由促肾上腺皮质激素释放因子（CRF）介导的疾病中的应用。