N-tert-Butyl-N'-<6-(4-chlorophenoxy)-2,4-diisopropylpyrid-3-yl>thiourea | 133979-17-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: N-tert-Butyl-N'-<6-(4-chlorophenoxy)-2,4-diisopropylpyrid-3-yl>thiourea
• 英文别名: 1-tert-butyl-3-[2,4-diisopropyl-6-(4-chlorophenoxy)-pyrid-3-yl]-thiourea；1-tert.-Butyl-3-[2,4-diisopropyl-6-(4-chlorophenoxy)-pyrid-3-yl]-thiourea；1-tert-butyl-3-[6-(4-chlorophenoxy)-2,4-di(propan-2-yl)pyridin-3-yl]thiourea
• CAS: 133979-17-6
• 化学式: C₂₂H₃₀ClN₃OS
• 分子量: 420.019
• InChiKey: SOSVWTKXLHSAOI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.2
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  78.3
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-tert-Butyl-N'-<6-(4-chlorophenoxy)-2,4-diisopropylpyrid-3-yl>thiourea 在 2-氯-1-甲基吡啶碘化物 、 三乙胺 作用下， 以 乙腈 为溶剂， 以98%的产率得到1-tert.-butyl-3-[2,4-diisopropyl-6-(4-chlorophenoxy)-pyrid-3-yl]-carbodiimide
  参考文献：
  名称：

  N-(pyrid-3-yl)thioureas and derivatives as acaricides. I. Synthesis and biological properties

  摘要：

  AbstractIn the course of optimization studies around diafenthiuron, the central aromatic nucleus linked directly to the thiourea unit was replaced by a pyridine moiety. A series of N‐(pyrid‐3‐yl)thioureas, ‐isothioureas and ‐carbodiimides was synthesised and evaluated for acaricidal activity. The synthetic methodology used and the screening results against some spider mites (Tetranychus spp. and Panonychus ssp.) are discussed.

  DOI：

  10.1002/ps.2780420402
• 作为产物：
  描述：

  6-(4-Chlorophenoxy)-2,4-diisopropylpyridine-3-amine 在 三乙胺 作用下， 以 吡啶 、 甲苯 为溶剂， 反应 31.0h， 生成 N-tert-Butyl-N'-<6-(4-chlorophenoxy)-2,4-diisopropylpyrid-3-yl>thiourea
  参考文献：
  名称：

  N-(pyrid-3-yl)thioureas and derivatives as acaricides. I. Synthesis and biological properties

  摘要：

  AbstractIn the course of optimization studies around diafenthiuron, the central aromatic nucleus linked directly to the thiourea unit was replaced by a pyridine moiety. A series of N‐(pyrid‐3‐yl)thioureas, ‐isothioureas and ‐carbodiimides was synthesised and evaluated for acaricidal activity. The synthetic methodology used and the screening results against some spider mites (Tetranychus spp. and Panonychus ssp.) are discussed.

  DOI：

  10.1002/ps.2780420402

文献信息

• Aminopyridines
  申请人：Ciba-Geigy Corporation

  公开号：US05077304A1

  公开（公告）日：1991-12-31

  Novel 3-amino-2,4-dialkylpyridine derivatives ##STR1## in which R.sup.1 and R.sup.2 are each independently C.sub.1 -C.sub.6 alkyl, R.sup.3 is C.sub.1 -C.sub.12 alkyl, C.sub.3 -C.sub.6 cycloalkyl, C.sub.1 -C.sub.4 alkyl substituted by C.sub.3 -C.sub.6 cycloalkyl, or C.sub.3 -C.sub.6 cycloalkyl substituted by C.sub.1 -C.sub.4 alkyl, R.sup.4 is hydrogen, halogen, C.sub.1 -C.sub.6 alkyl, phenoxy, or phenoxy that is mono- or di-substituted by halogen, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkylthio, C.sub.1 -C.sub.4 alkylamino, di-C.sub.1 -C.sub.4 alkylamino, C.sub.1 -C.sub.4 alkylcarbonylamino, C.sub.1 -C.sub.4 alkylcarbonyl, benzoyl, nitro, cyano, C.sub.1 -C.sub.4 alkoxycarbonyl, C.sub.1 -C.sub.4 haloalkyl or by C.sub.1 -C.sub.4 haloalkoxy, and Z is a bridge member --NH--CS--NH--, --N.dbd.C(SR.sup.5)--NH-- or --N.dbd.C.dbd.N-- wherein R.sup.5 is C.sub.1 -C.sub.6 alkyl or C.sub.3 -C.sub.5 alkenyl, can be used as pesticides. Preferably, insects and arachnids can be controlled.

  新型3-氨基-2,4-二烷基吡啶衍生物##STR1##中，其中R.sup.1和R.sup.2分别独立为C.sub.1-C.sub.6烷基，R.sup.3为C.sub.1-C.sub.12烷基，C.sub.3-C.sub.6环烷基，C.sub.1-C.sub.4被C.sub.3-C.sub.6环烷基取代的烷基，或C.sub.3-C.sub.6环烷基被C.sub.1-C.sub.4烷基取代，R.sup.4为氢，卤素，C.sub.1-C.sub.6烷基，苯氧基，或被卤素，C.sub.1-C.sub.4烷基，C.sub.1-C.sub.4烷氧基，C.sub.1-C.sub.4烷硫基，C.sub.1-C.sub.4烷基氨基，二C.sub.1-C.sub.4烷基氨基，C.sub.1-C.sub.4烷基羰基氨基，C.sub.1-C.sub.4烷基羰基，苯甲酰基，硝基，氰基，C.sub.1-C.sub.4烷氧羰基，C.sub.1-C.sub.4卤代烷基或C.sub.1-C.sub.4卤代烷氧基取代的苯氧基，Z为桥接成员--NH--CS--NH--，--N.dbd.C(SR.sup.5)--NH--或--N.dbd.C.dbd.N--其中R.sup.5为C.sub.1-C.sub.6烷基或C.sub.3-C.sub.5烯基，可用作杀虫剂。最好是可以控制昆虫和蛛形动物。
• US5077304A
  申请人：——

  公开号：US5077304A

  公开（公告）日：1991-12-31
• <i>N</i>-(pyrid-3-yl)thioureas and derivatives as acaricides. I. Synthesis and biological properties
  作者：Alfons Pascual、Alfred Rindlisbacher

  DOI：10.1002/ps.2780420402

  日期：1994.12

  AbstractIn the course of optimization studies around diafenthiuron, the central aromatic nucleus linked directly to the thiourea unit was replaced by a pyridine moiety. A series of N‐(pyrid‐3‐yl)thioureas, ‐isothioureas and ‐carbodiimides was synthesised and evaluated for acaricidal activity. The synthetic methodology used and the screening results against some spider mites (Tetranychus spp. and Panonychus ssp.) are discussed.