6-Chloro-3-nitro-2-propoxypyridine | 1094676-15-9

• 分子结构分类: 有机化合物 - 有机1,3-偶极化合物 - 烯丙基型1,3-偶极有机化合物
• 英文名称: 6-Chloro-3-nitro-2-propoxypyridine
• CAS: 1094676-15-9
• 化学式: C₈H₉ClN₂O₃
• 分子量: 216.624
• InChiKey: AGWITSFMXJIDII-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  67.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-{2,6-二氯-4-[(3,3-二氯-2-丙烯-1-基)氧基]苯氧基}-1-丙醇 、 6-Chloro-3-nitro-2-propoxypyridine 以 四氢呋喃 为溶剂， 生成 6-(3-{2,6-dichloro-4-[(3,3-dichloroprop-2-en-1-yl)oxy]phenoxy}propoxy)-3-nitro-2-propoxypyridine
  参考文献：
  名称：

  Synthesis and Insecticidal Activity of Novel Nitropyridyl-Based Dichloropropene Ethers

  摘要：

  Dihalopropene ether insecticides are known for good features such as no cross-resistance to other insecticide classes and safety for mammals. Pyridalyl is the only currently commercialized dichloropropene ether insecticide; however, it contains a trifluoromethyl group, the synthesis of which requires harsh reagents and reaction conditions. To search for novel dihalopropene ethers with unique biological activities but without trifluoromethyl groups, a series of nitropyridyl-based dichloropropene ether analogues were synthesized by reacting nitro-based halopyridine with 2,6-dichloro-4-(3,3-dichloroallyloxy)phenol or 2,6-dichloro-4-(3,3-dichloroallyloxy)phenyl 3-hydroxypropyl ether. Bioassay showed that the compounds exhibited potent insecticidal activities against various lepidopteran pests. Particularly, 2,6-dichloro-4-(3,3-dichloroallyloxy)phenyl 3-(5-nitro-2-pyridyloxy)propyl ether (8e) was active against major agricultural pests, and its insecticidal potency was comparable to that of Pyridalyl. Besides the trifluoromethyl group in Pyridalyl, a nitro group on the 5-position of the pyridyl ring is also viable for the development of optimal insecticidal activity.

  DOI：

  10.1021/acs.jafc.5b02279
• 作为产物：
  描述：

  1-碘代丙烷 、 6-氯-3-硝基吡啶-2-醇 在 silver carbonate 作用下， 以 正己烷 为溶剂， 反应 0.17h， 以88%的产率得到6-Chloro-3-nitro-2-propoxypyridine
  参考文献：
  名称：

  Microwave-Assisted Silver(I)-Mediated Selective O-Alkylation of Aromatic Imidate Systems

  摘要：

  一种新颖的微波辅助协议已被开发，用于在微波辐照下使用碳酸银作为碱，对芳香咪唑酰胺体系进行选择性O-烷基化，反应时间短且产率优异。

  DOI：

  10.1055/s-0029-1216878

文献信息

• Synthesis and Insecticidal Activity of Novel Nitropyridyl-Based Dichloropropene Ethers
  作者：Aiping Liu、Wanqi Yu、Minhua Liu、Jianjun Bai、Weidong Liu、Xingping Liu、Hui Pei、Li Hu、Mingzhi Huang、Xiaoguang Wang

  DOI：10.1021/acs.jafc.5b02279

  日期：2015.9.2

  Dihalopropene ether insecticides are known for good features such as no cross-resistance to other insecticide classes and safety for mammals. Pyridalyl is the only currently commercialized dichloropropene ether insecticide; however, it contains a trifluoromethyl group, the synthesis of which requires harsh reagents and reaction conditions. To search for novel dihalopropene ethers with unique biological activities but without trifluoromethyl groups, a series of nitropyridyl-based dichloropropene ether analogues were synthesized by reacting nitro-based halopyridine with 2,6-dichloro-4-(3,3-dichloroallyloxy)phenol or 2,6-dichloro-4-(3,3-dichloroallyloxy)phenyl 3-hydroxypropyl ether. Bioassay showed that the compounds exhibited potent insecticidal activities against various lepidopteran pests. Particularly, 2,6-dichloro-4-(3,3-dichloroallyloxy)phenyl 3-(5-nitro-2-pyridyloxy)propyl ether (8e) was active against major agricultural pests, and its insecticidal potency was comparable to that of Pyridalyl. Besides the trifluoromethyl group in Pyridalyl, a nitro group on the 5-position of the pyridyl ring is also viable for the development of optimal insecticidal activity.
• Microwave-Assisted Silver(I)-Mediated Selective O-Alkylation of Aromatic Imidate Systems
  作者：Erik Van der Eycken、Brajendra Singh、Claudia Cavalluzzo、Marc De Maeyer、Zeger Debyser、Virinder Parmar

  DOI：10.1055/s-0029-1216878

  日期：——

  A novel microwave-assisted protocol has been developed for the selective O-alkylation of aromatic imidate systems with various halides under microwave irradiation using silver carbonate as the base. Products were obtained in short reaction time and in excellent yields.

  一种新颖的微波辅助协议已被开发，用于在微波辐照下使用碳酸银作为碱，对芳香咪唑酰胺体系进行选择性O-烷基化，反应时间短且产率优异。