2-(6-Morpholin-4-ylpyridazin-3-yl)-2-phenylacetonitrile | 717876-14-7

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 2-(6-Morpholin-4-ylpyridazin-3-yl)-2-phenylacetonitrile
• CAS: 717876-14-7
• 化学式: C₁₆H₁₆N₄O
• 分子量: 280.329
• InChiKey: AKDTVSBSWNKYCZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  21
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  62
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-(6-Morpholin-4-ylpyridazin-3-yl)-2-phenylacetonitrile 在 吡啶 、 ammonium polysulfide 作用下， 反应 12.0h， 以63%的产率得到2-(6-Morpholin-4-ylpyridazin-3-yl)-2-phenylethanethioamide
  参考文献：
  名称：

  Synthesis, Fungicidal and Antibacterial Activity of New Pyridazine Derivatives

  摘要：

  Compounds 1 - 3 were obtained in the reaction of 3,6-dichloropyridazines with phenylacetonitriles in the biphasic system - DMSO / 50% NaOH. The chlorine atom was replaced with cycloalkylamino (4 - 13) and hydrazinyl (23, 24) moiety. These last compounds were condensed with aldehydes (25 - 34). Pyridazynylphenylacetonitriles were converted into amides 14 - 18 and thioamides 19 - 22. In compounds 2, 3 the chlorine atom was replaced with thiophenyl (37, 38) and in compound 1 with thioethyl and thiophenyl (35, 36) functional groups. In the reactions of compounds 1, 2 with ammonium polysulfide thioamides with thiol group (39, 40) and chlorine atom (41, 42) were obtained. Compounds 1 - 17, 19 43 were screened for antibacterial and fungicidal activities.

  DOI：

  10.3987/com-08-11577
• 作为产物：
  描述：

  吗啉 、 6-氯-α-苯基-3-哒嗪乙酰腈 以 1,4-二氧六环 为溶剂， 反应 2.0h， 以63%的产率得到2-(6-Morpholin-4-ylpyridazin-3-yl)-2-phenylacetonitrile
  参考文献：
  名称：

  Synthesis, Fungicidal and Antibacterial Activity of New Pyridazine Derivatives

  摘要：

  Compounds 1 - 3 were obtained in the reaction of 3,6-dichloropyridazines with phenylacetonitriles in the biphasic system - DMSO / 50% NaOH. The chlorine atom was replaced with cycloalkylamino (4 - 13) and hydrazinyl (23, 24) moiety. These last compounds were condensed with aldehydes (25 - 34). Pyridazynylphenylacetonitriles were converted into amides 14 - 18 and thioamides 19 - 22. In compounds 2, 3 the chlorine atom was replaced with thiophenyl (37, 38) and in compound 1 with thioethyl and thiophenyl (35, 36) functional groups. In the reactions of compounds 1, 2 with ammonium polysulfide thioamides with thiol group (39, 40) and chlorine atom (41, 42) were obtained. Compounds 1 - 17, 19 43 were screened for antibacterial and fungicidal activities.

  DOI：

  10.3987/com-08-11577

文献信息

• Synthesis, Fungicidal and Antibacterial Activity of New Pyridazine Derivatives
  作者：Henryk Foks、Krystyna Wisterowicz、Agnieszka Miszke、Kamil Brożewicz、Katarzyna Wiśniewska、Maria Dąbrowska-Szponar

  DOI：10.3987/com-08-11577

  日期：——

  Compounds 1 - 3 were obtained in the reaction of 3,6-dichloropyridazines with phenylacetonitriles in the biphasic system - DMSO / 50% NaOH. The chlorine atom was replaced with cycloalkylamino (4 - 13) and hydrazinyl (23, 24) moiety. These last compounds were condensed with aldehydes (25 - 34). Pyridazynylphenylacetonitriles were converted into amides 14 - 18 and thioamides 19 - 22. In compounds 2, 3 the chlorine atom was replaced with thiophenyl (37, 38) and in compound 1 with thioethyl and thiophenyl (35, 36) functional groups. In the reactions of compounds 1, 2 with ammonium polysulfide thioamides with thiol group (39, 40) and chlorine atom (41, 42) were obtained. Compounds 1 - 17, 19 43 were screened for antibacterial and fungicidal activities.