6-氟-4-氧代-1,4-二氢-3-喹啉甲腈 | 71083-60-8

• 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
• 中文名称: 6-氟-4-氧代-1,4-二氢-3-喹啉甲腈
• 英文名称: 6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbonitrile
• 英文别名: 6-fluoro-4-oxo-1H-quinoline-3-carbonitrile
• CAS: 71083-60-8
• 化学式: C₁₀H₅FN₂O
• mdl: MFCD09948131
• 分子量: 188.161
• InChiKey: BHNUHFWMNOYIAE-UHFFFAOYSA-N

物化性质

• 沸点：
  304.5±42.0 °C(Predicted)
• 密度：
  1.41±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  14
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  52.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  6-氟-4-氧代-1,4-二氢-3-喹啉甲腈 在 三氯氧磷 作用下， 反应 0.5h， 生成 4-氯-6-氟-喹啉-3-甲腈
  参考文献：
  名称：

  Discovery of VU6027459: A First-in-Class Selective and CNS Penetrant mGlu₇ Positive Allosteric Modulator Tool Compound

  摘要：

  Herein, we report the discovery of the first selective and CNS penetrant mGlu(7) PAM (VU6027459) derived from a "molecular switch" within a selective mGlu(7) NAM chemotype. VU6027459 displayed CNS penetration in both mice (K-p = 2.74) and rats (K-p = 4.78), it was orally bioavailable in rats (%F = 69.5), and undesired activity at DAT was ablated.

  DOI：

  10.1021/acsmedchemlett.0c00432
• 作为产物：
  描述：

  2-氨基-5-氟苯甲酸 在 正丁基锂 作用下， 以 四氢呋喃 、 甲醇 、 benzine 、 正己烷 为溶剂， 反应 2.5h， 生成 6-氟-4-氧代-1,4-二氢-3-喹啉甲腈
  参考文献：
  名称：

  Discovery of VU6027459: A First-in-Class Selective and CNS Penetrant mGlu₇ Positive Allosteric Modulator Tool Compound

  摘要：

  Herein, we report the discovery of the first selective and CNS penetrant mGlu(7) PAM (VU6027459) derived from a "molecular switch" within a selective mGlu(7) NAM chemotype. VU6027459 displayed CNS penetration in both mice (K-p = 2.74) and rats (K-p = 4.78), it was orally bioavailable in rats (%F = 69.5), and undesired activity at DAT was ablated.

  DOI：

  10.1021/acsmedchemlett.0c00432

文献信息

• Copper‐Catalyzed Synthesis of Substituted 4‐Quinolones using Water as a Benign Reaction Media: Application for the Construction of Oxolinic Acid and BQCA
  作者：Babasaheb Sopan Gore、Chein Chung Lee、Jessica Lee、Jeh‐Jeng Wang

  DOI：10.1002/adsc.201900286

  日期：2019.7.11

  −NO2, −SO2Ar, and −COAr were also successful. In addition, reaction with heterocyclic compounds such as 3‐(3‐bromothiophen‐2‐yl)‐3‐oxopropanenitrile proceeded smoothly to afford tetrahydrothieno[3,2‐b]pyridine‐6‐carbonitrile analogues. The practicality of the designed protocol was confirmed by gram scale synthesis of two derivatives.

  已开发出一种铜催化的三组分合成方法，用于从取代的3-（2-卤代苯基）-3-氧代丙烷，醛和水溶液合成取代的4-喹诺酮衍生物。NH 3使用水作为对环境无害的反应介质。此外，所获得产品的合成效用已成功地用于合成可用的亚氧酸和BQCA药物。该方法的关键特征包括可商购的起始原料，广泛的范围以及中等至良好的反应产率。与甲醛反应，以及其他官能团，例如-CN，-NO 2，-SO 2Ar和-COAr也成功。此外，与杂环化合物（如3-（3-溴噻吩-2-基）-3-氧代丙烷腈）的反应进行得很顺利，得到了四氢噻吩并[3,2 - b ]吡啶-6-腈的类似物。两种衍生物的克级合成证实了所设计方案的实用性。
• Synthesis and cytotoxicity studies of quinoline-3-carbonitrile derivatives
  作者：Shu Lan Zhang、Xin Zhai、Shi Jiao Zhang、Hong Hao Yu、Ping Gong

  DOI：10.1016/j.cclet.2010.03.016

  日期：2010.8

  A series of quinoline-3-carbonitrile derivatives were designed and synthesized. Their cytotoxicity in vitro against four cancer cell lines (A549, HT-29, MDA-MB-231 and SMMC-7721) were evaluated by standard MTT assay. The pharmacological results showed that most of the prepared compounds displayed excellent selective cytotoxicity toward SMMC-7721 cell line. Among them, compounds 7c, 7e, 11b, 11f and 11g were more active than Gefitinb against SMMC-7721 cell line. (C) 2010 Ping Gong. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.