摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

13-Chloro-2,4,9,17-tetrazatetracyclo[8.7.0.03,8.011,16]heptadeca-1,3(8),4,6,9,11(16),12,14-octaene | 1621885-01-5

中文名称
——
中文别名
——
英文名称
13-Chloro-2,4,9,17-tetrazatetracyclo[8.7.0.03,8.011,16]heptadeca-1,3(8),4,6,9,11(16),12,14-octaene
英文别名
13-chloro-2,4,9,17-tetrazatetracyclo[8.7.0.03,8.011,16]heptadeca-1,3(8),4,6,9,11(16),12,14-octaene
13-Chloro-2,4,9,17-tetrazatetracyclo[8.7.0.03,8.011,16]heptadeca-1,3(8),4,6,9,11(16),12,14-octaene化学式
CAS
1621885-01-5
化学式
C13H7ClN4
mdl
——
分子量
254.678
InChiKey
HHXOUHKZKHBPTR-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    54.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2,3-二氨基吡啶5-氯靛红乙二醇 为溶剂, 反应 0.2h, 以97%的产率得到13-Chloro-2,4,9,17-tetrazatetracyclo[8.7.0.03,8.011,16]heptadeca-1,3(8),4,6,9,11(16),12,14-octaene
    参考文献:
    名称:
    Cu doped CdS nanoparticles: A versatile and recoverable catalyst for chemoselective synthesis of indolo[2,3- b ]quinoxaline derivatives under microwave irradiation
    摘要:
    CdS and Cu doped CdS NPs has been obtained successfully using safe agents through a simple aqueous chemical method and characterized by XRD, TEM, SEM, EDAX, UV/VIS and ICP-AES. These investigations revealed that the particle size of the synthesized materials were uniformly distributed in the range of 2-4 nm and confirm the Cu doping in the lattice of CdS NPs. These nanoparticles were exploited to study their catalytic activities toward the chemoselective synthesis of indolo[2,3-blquinoxalines by the reaction of isatins with 1,2-diamines in ethylene glycol under microwave irradiation. The method showed remarkable selectivity for indolo[2,3-b]quinoxalines over 3-imino-isatin, spirobenzimidazole, and ring-opened quinoxalinone derivatives. The catalytic activity of Cu doped CdS NPs was found to be about 18-fold higher under microwave irradiation (MW) as compared to the conventional method. Nanocatalyst plays a dual role of catalyst as well as susceptor, and enhances the overall capacity to absorb MW in the reaction mixture. Doping of Cu promotes the activity and selectivity of CdS nanoparticles indicated by high TOF value with good chemoselectivity. The surface acidity of NPs was measured by FTIR spectra of chemisorbed pyridine. Simple workup, mild reaction conditions, low cost, easy separation, and reusability of the catalyst are some advantages of this method. (C) 2014 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.molcata.2014.07.022
点击查看最新优质反应信息

文献信息

  • Cu doped CdS nanoparticles: A versatile and recoverable catalyst for chemoselective synthesis of indolo[2,3- b ]quinoxaline derivatives under microwave irradiation
    作者:Anshu Dandia、Vijay Parewa、Shuchi Maheshwari、Kuldeep S. Rathore
    DOI:10.1016/j.molcata.2014.07.022
    日期:2014.11
    CdS and Cu doped CdS NPs has been obtained successfully using safe agents through a simple aqueous chemical method and characterized by XRD, TEM, SEM, EDAX, UV/VIS and ICP-AES. These investigations revealed that the particle size of the synthesized materials were uniformly distributed in the range of 2-4 nm and confirm the Cu doping in the lattice of CdS NPs. These nanoparticles were exploited to study their catalytic activities toward the chemoselective synthesis of indolo[2,3-blquinoxalines by the reaction of isatins with 1,2-diamines in ethylene glycol under microwave irradiation. The method showed remarkable selectivity for indolo[2,3-b]quinoxalines over 3-imino-isatin, spirobenzimidazole, and ring-opened quinoxalinone derivatives. The catalytic activity of Cu doped CdS NPs was found to be about 18-fold higher under microwave irradiation (MW) as compared to the conventional method. Nanocatalyst plays a dual role of catalyst as well as susceptor, and enhances the overall capacity to absorb MW in the reaction mixture. Doping of Cu promotes the activity and selectivity of CdS nanoparticles indicated by high TOF value with good chemoselectivity. The surface acidity of NPs was measured by FTIR spectra of chemisorbed pyridine. Simple workup, mild reaction conditions, low cost, easy separation, and reusability of the catalyst are some advantages of this method. (C) 2014 Elsevier B.V. All rights reserved.
查看更多

同类化合物

氨甲酸,(5-氨基-2,3-二苯基吡啶并[3,4-b]吡嗪-7-基)-,乙基酯 咪唑并[1,5-a]吡啶并[3,2-e]吡嗪-6(5H)-酮 咪唑并[1,5-A]吡啶并[2,3-E]吡嗪-4(5H)-酮 咪唑并[1,2-a]吡啶并[3,2-E]吡嗪-6-醇 咪唑并[1,2-a]吡啶并[2,3-E]吡嗪-4(5H)-酮 吡啶并[3,4-b]吡嗪-7-胺 吡啶并[3,4-b]吡嗪-3(4h)-酮 吡啶并[3,4-b]吡嗪-2,3(1H,4H)-二酮 吡啶并[2,3-b]吡嗪-7-基硼酸频那醇酯 吡啶并[2,3-b]吡嗪-6(5H)-酮 吡啶并[2,3-b]吡嗪-2-羧酸 吡啶并[2,3-b]吡嗪-2(1h)-酮 吡啶并[2,3-b]吡嗪-2(1H)-酮,3,6-二甲基-(9CI) 吡啶并[2,3-B]吡嗪-8-甲醛 吡啶并[2,3-B]吡嗪-6-胺 吡啶并[2,3-B]吡嗪-6-羧酸 乙基[3-(4-氯苯基)-8-{[5-(二乙胺基)戊烷-2-基]氨基}吡啶并[2,3-b]吡嗪-6-基]氨基甲酸酯 乙基4-甲基-3-羰基-3,4-二氢吡啶并[2,3-b]吡嗪-2-羧酸酯 乙基(8-amino-2-{[methyl(phenyl)amino]methyl}pyrido[2,3-b]pyrazin-6-yl)氨基甲酸酯 N-乙基-N'-[3-[(4-甲基苯基)氨基]吡啶并[2,3-B]吡嗪-6-基]脲 N-[3-(4-羟基苯基)吡啶并[2,3-b]吡嗪-6-基]-N'-2-丙烯-1-基硫脲 8-甲基吡啶并[2,3-b]吡嗪 8-溴吡啶并[3,4-b]吡嗪 8-氯吡喃并[3,4-b]吡嗪 7-碘-吡啶并[2,3-b]吡嗪 7-硝基吡啶并[2,3-b]吡嗪 7-溴吡啶并[2,3-b]吡嗪 7-溴吡啶并[2,3-B]吡嗪-2,3(1H,4H)-二酮 7-溴-8-甲基吡啶并[2,3-B〕吡嗪 7-溴-6-甲基吡啶并[2,3-B]吡嗪 7-溴-2-甲基吡啶并[2,3-B]吡嗪 7-溴-2,3-二甲基吡啶并[2,3-b]吡嗪 7-氯吡啶并[3,4-b]吡嗪 7-氯-1,4-二氢吡啶并[2,3-B]吡嗪-2,3-二酮 7-氯-1,4-二氢-1-(2-丙氧乙基)-吡啶并[3,4-b]吡嗪-2,3-二酮 7-氨基吡啶并[2,3-B]吡嗪 6-肼基-3-苯基吡啶并[2,3-b]吡嗪-2-醇 6-甲氧基吡啶并[2,3-b]吡嗪-3(4h)-酮 6-溴吡啶并[2,3-B]吡嗪 6-氯咪唑并[1,5-a]吡啶并[3,2-e]吡嗪 6-氯吡啶并[3,2-B]吡嗪 6-氯吡啶并[2,3-b]吡嗪-2(1H)-酮 6-氯吡啶并[2,3-B]吡嗪-3(4H)-酮 6-氨基-3-羟基-吡啶并[2,3-B]吡嗪-2-羧酸 5-氯-吡啶[3,4-B]吡嗪 5,8-二氢-环丁[b]吡啶并[3,4-e]吡嗪-6,7-二酮 5,8-二氢-环丁[b]吡啶并[2,3-e]吡嗪-6,7-二酮 5,7-二氯吡啶并[4,3-b]吡嗪 4H-吡啶并[2,3-b]吡嗪-3-酮 4-(2,2-二甲基-1,3-二噁烷-5-基)-6-甲氧基吡啶并[2,3-B]吡嗪-3(4H)-酮