N-(6-methylpyrid-2-yl)-N-(4-methylquinolin-2-yl)acetamide | 342653-91-2

• 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
• 英文名称: N-(6-methylpyrid-2-yl)-N-(4-methylquinolin-2-yl)acetamide
• 英文别名: N-(6-Methylpyridin-2-yl)-N-(4-methylquinolin-2-yl)acetamide
• CAS: 342653-91-2
• 化学式: C₁₈H₁₇N₃O
• 分子量: 291.352
• InChiKey: QADPHTWXQYVDMA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  22
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  46.1
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  palladium dichloride 、 N-(6-methylpyrid-2-yl)-N-(4-methylquinolin-2-yl)acetamide 在 HCl 作用下， 以 甲醇 、 水 为溶剂， 以83%的产率得到N-acetyl-N-(6-methylpyrid-2-yl)-N-(4-methylquinolin-2-yl)amine palladium dichloride
  参考文献：
  名称：

  N-Acyl-N,N-dipyridyl and N-acyl-N-pyridyl-N-quinoyl amine based palladium complexes. Synthesis, X-ray structures, heterogenization and use in Heck couplings

  摘要：

  A series of homogeneous and heterogeneous palladium(II)-catalysts and their use in Heck-couplings is described. Starting from four different amines, N-pyrid-2-yl-N-(3-methylpyrid-2-yl) amine (1), N-pyrid-2-yl-N-(6-methylpyrid-2-yl) amine (2), N-(6-methylpyrid-2-yl)-N-(4-methylquinolin-2-yl)amine (3) and N-bis (6-methylpyrid-2-yl) amine (4), the corresponding acetyl- and norbornene derivatives, N-pyrid-2-yl-N-(3-methylpyrid-2-yl) acetamide (5), N-pyrid-2-yl-N-(6-methylpyrid-2-yl) acetamide (6), N-(6-methylpyrid-2-yl) -N-(4-methylquinolin-2-yl) acetamide (7), N-bis (6-methylpyrid-2-yl) acetamide (8) and N-pyrid-2-yl-N-(3-methylpyrid-2-yl)-endo-norborn-2-ene-5-carbamide (9), N-pyrid-2-yl-N-(6-methylpyrid-2-yl)-endo-norborn-2-ene-5-carbamide (10) and N-(6-methylpyrid-2-yl) -N-(4-methylquinolin-2-yl)-endo-norborn-2-ene-5-carbamide (11), respectively, have been prepared. The acetyl derivatives 5-8 have been used for the preparation of the homogeneous Heck catalysts N-acetyl-N-pyrid-2-yl-N-(3-methylpyrid-2-yl)amine palladium dichloride (13), N-acetyl-N-pyrid-2-yl-N-(6-methylpyrid-2-yl) amine palladium dichloride (14), N-acetyl-N-(6-methylpyrid-2-yl)-N- (4-methylquinolin-2-yl) amine palladium dichloride (15) and N-acetyl-N-bis(6-methylpyrid-2-yl)amine palladium dichloride (16). X-ray data were obtained for compounds 9, 11, 13 and 14. Polymer supports 17-19 were prepared via ring-opening metathesis copolymerization of the norbornene derivatives 9-11 with 1,4,4a,5,8,8a-hexahydro-1,4,5,8-exo-endo-dimethano-naphthalene (HDMN-6) and subsequently loaded with palladium(II) chloride. Both the homogeneous catalysts 13-16 and the heterogeneous catalysts are active in the vinylation of aryl iodides and aryl bromides with turn-over numbers (TONs) of up to 220 000. Comparably low yields (= 34%) and TONs (= 2100) are achieved in the tetrabutylammonium bromide- (TBAB-) assisted vinylation of aryl chlorides as well as in the amination of aryl bromides. Structural data of compounds 9, 11, 13 and 14 were compared with those of the parent systems, N-acetyldipyridylamine palladiumdichloride (20) and the poly(N,N-dipyrid-2-yl-endo-norborn-2-ene-5-carbamide)based resin (21), respectively. Thus, methyl-substitution leads to a significant perturbation of the almost perfect square planar coordination of Pd found in 20 resulting in lowered stabilities of the corresponding Pd-complexes 13-16 and consequently lowered coupling yields compared to 20 and 21. (C) 2001 Elsevier Science B.V. All rights reserved.

  DOI：

  10.1016/s0022-328x(00)00783-x
• 作为产物：
  描述：

  4-甲基-2-氯-喹啉 在 tris-(dibenzylideneacetone)dipalladium(0) 二苯基丙基膦 、 sodium t-butanolate 作用下， 以 甲苯 为溶剂， 反应 4.0h， 生成 N-(6-methylpyrid-2-yl)-N-(4-methylquinolin-2-yl)acetamide
  参考文献：
  名称：

  N-Acyl-N,N-dipyridyl and N-acyl-N-pyridyl-N-quinoyl amine based palladium complexes. Synthesis, X-ray structures, heterogenization and use in Heck couplings

  摘要：

  A series of homogeneous and heterogeneous palladium(II)-catalysts and their use in Heck-couplings is described. Starting from four different amines, N-pyrid-2-yl-N-(3-methylpyrid-2-yl) amine (1), N-pyrid-2-yl-N-(6-methylpyrid-2-yl) amine (2), N-(6-methylpyrid-2-yl)-N-(4-methylquinolin-2-yl)amine (3) and N-bis (6-methylpyrid-2-yl) amine (4), the corresponding acetyl- and norbornene derivatives, N-pyrid-2-yl-N-(3-methylpyrid-2-yl) acetamide (5), N-pyrid-2-yl-N-(6-methylpyrid-2-yl) acetamide (6), N-(6-methylpyrid-2-yl) -N-(4-methylquinolin-2-yl) acetamide (7), N-bis (6-methylpyrid-2-yl) acetamide (8) and N-pyrid-2-yl-N-(3-methylpyrid-2-yl)-endo-norborn-2-ene-5-carbamide (9), N-pyrid-2-yl-N-(6-methylpyrid-2-yl)-endo-norborn-2-ene-5-carbamide (10) and N-(6-methylpyrid-2-yl) -N-(4-methylquinolin-2-yl)-endo-norborn-2-ene-5-carbamide (11), respectively, have been prepared. The acetyl derivatives 5-8 have been used for the preparation of the homogeneous Heck catalysts N-acetyl-N-pyrid-2-yl-N-(3-methylpyrid-2-yl)amine palladium dichloride (13), N-acetyl-N-pyrid-2-yl-N-(6-methylpyrid-2-yl) amine palladium dichloride (14), N-acetyl-N-(6-methylpyrid-2-yl)-N- (4-methylquinolin-2-yl) amine palladium dichloride (15) and N-acetyl-N-bis(6-methylpyrid-2-yl)amine palladium dichloride (16). X-ray data were obtained for compounds 9, 11, 13 and 14. Polymer supports 17-19 were prepared via ring-opening metathesis copolymerization of the norbornene derivatives 9-11 with 1,4,4a,5,8,8a-hexahydro-1,4,5,8-exo-endo-dimethano-naphthalene (HDMN-6) and subsequently loaded with palladium(II) chloride. Both the homogeneous catalysts 13-16 and the heterogeneous catalysts are active in the vinylation of aryl iodides and aryl bromides with turn-over numbers (TONs) of up to 220 000. Comparably low yields (= 34%) and TONs (= 2100) are achieved in the tetrabutylammonium bromide- (TBAB-) assisted vinylation of aryl chlorides as well as in the amination of aryl bromides. Structural data of compounds 9, 11, 13 and 14 were compared with those of the parent systems, N-acetyldipyridylamine palladiumdichloride (20) and the poly(N,N-dipyrid-2-yl-endo-norborn-2-ene-5-carbamide)based resin (21), respectively. Thus, methyl-substitution leads to a significant perturbation of the almost perfect square planar coordination of Pd found in 20 resulting in lowered stabilities of the corresponding Pd-complexes 13-16 and consequently lowered coupling yields compared to 20 and 21. (C) 2001 Elsevier Science B.V. All rights reserved.

  DOI：

  10.1016/s0022-328x(00)00783-x