1-Iodo-2-naphthalenecarbonyl chloride | 1261657-85-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 1-Iodo-2-naphthalenecarbonyl chloride
• 英文别名: 1-iodonaphthalene-2-carbonyl chloride
• CAS: 1261657-85-5
• 化学式: C₁₁H₆ClIO
• 分子量: 316.526
• InChiKey: RLOLCTGQVSNDRJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-Iodo-2-naphthalenecarbonyl chloride 、 邻氯苯胺 在 吡啶 作用下， 以 二氯甲烷 为溶剂， 生成 N-(2-chlorophenyl)-1-iodo-2-naphthamide
  参考文献：
  名称：

  Dibenzodiazepinones的合成通过串联铜（I） -催化CN键的形成

  摘要：

  AbstractAn efficient, one‐pot method for the synthesis of dibenzodiazepinone derivatives involving copper‐catalyzed tandem CN bond formation is reported. The use of various halo amide and 2‐iodoaniline derivatives permitted the synthesis of an array of dibenzodiazepinone derivatives in moderate to good yields. Moreover, a dibenzodiazepinone derivative {2‐(11‐oxo‐5H‐dibenzo[b,e][1,4]diazepin‐10(11H)‐yl)benzonitrile} was utilized to synthesize the triazapentacyclic ring derivative {12‐chloro‐ 8,15,22‐triazapentacyclo[13.7.0.02,7.09,14.016,21]docosa‐1(22),2,4,6,9(14),10,12,16(21),17,19‐decaene}.magnified image

  DOI：

  10.1002/adsc.201301020
• 作为产物：
  描述：

  1-碘-2-萘甲酸 在 氯化亚砜 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 3.0h， 生成 1-Iodo-2-naphthalenecarbonyl chloride
  参考文献：
  名称：

  Dibenzodiazepinones的合成通过串联铜（I） -催化CN键的形成

  摘要：

  AbstractAn efficient, one‐pot method for the synthesis of dibenzodiazepinone derivatives involving copper‐catalyzed tandem CN bond formation is reported. The use of various halo amide and 2‐iodoaniline derivatives permitted the synthesis of an array of dibenzodiazepinone derivatives in moderate to good yields. Moreover, a dibenzodiazepinone derivative {2‐(11‐oxo‐5H‐dibenzo[b,e][1,4]diazepin‐10(11H)‐yl)benzonitrile} was utilized to synthesize the triazapentacyclic ring derivative {12‐chloro‐ 8,15,22‐triazapentacyclo[13.7.0.02,7.09,14.016,21]docosa‐1(22),2,4,6,9(14),10,12,16(21),17,19‐decaene}.magnified image

  DOI：

  10.1002/adsc.201301020

文献信息

• Synthesis of Dibenzodiazepinones<i>via</i>Tandem Copper(I)- Catalyzed CN Bond Formation
  作者：Sachin D. Gawande、Veerababurao Kavala、Manoj R. Zanwar、Chun-Wei Kuo、Wen-Chang Huang、Ting-Shen Kuo、Hsiu-Ni Huang、Chiu-Hui He、Ching-Fa Yao

  DOI：10.1002/adsc.201301020

  日期：2014.8.11

  AbstractAn efficient, one‐pot method for the synthesis of dibenzodiazepinone derivatives involving copper‐catalyzed tandem CN bond formation is reported. The use of various halo amide and 2‐iodoaniline derivatives permitted the synthesis of an array of dibenzodiazepinone derivatives in moderate to good yields. Moreover, a dibenzodiazepinone derivative 2‐(11‐oxo‐5H‐dibenzo[b,e][1,4]diazepin‐10(11H)‐yl)benzonitrile} was utilized to synthesize the triazapentacyclic ring derivative 12‐chloro‐ 8,15,22‐triazapentacyclo[13.7.0.02,7.09,14.016,21]docosa‐1(22),2,4,6,9(14),10,12,16(21),17,19‐decaene}.magnified image