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5-(4-chlorophenyl)-4-(4-(2,3-dichlorophenyl)piperazin-1-yl)thieno[2,3-d]pyrimidine-6-carbonitrile | 1446090-58-9

中文名称
——
中文别名
——
英文名称
5-(4-chlorophenyl)-4-(4-(2,3-dichlorophenyl)piperazin-1-yl)thieno[2,3-d]pyrimidine-6-carbonitrile
英文别名
5-(4-Chlorophenyl)-4-[4-(2,3-dichlorophenyl)piperazin-1-yl]thieno[2,3-d]pyrimidine-6-carbonitrile;5-(4-chlorophenyl)-4-[4-(2,3-dichlorophenyl)piperazin-1-yl]thieno[2,3-d]pyrimidine-6-carbonitrile
5-(4-chlorophenyl)-4-(4-(2,3-dichlorophenyl)piperazin-1-yl)thieno[2,3-d]pyrimidine-6-carbonitrile化学式
CAS
1446090-58-9
化学式
C23H16Cl3N5S
mdl
——
分子量
500.839
InChiKey
XLUUNCKDRKIJHO-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):
    7.2
  • 重原子数:
    32
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    84.3
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthetic tactics of new class of 4-aminothieno[2,3-d]pyrimidine-6-carbonitrile derivatives acting as antimicrobial agents
    摘要:
    Thermal selective reactions were studied on oxothieno[2,3-d]pyrimidine-6-carboxamide 3 with POCI3 and PCI5. At 25-50 degrees C, the C-7-amide rearranges to nitrile furnished compound 4 in 85-90% yield, while at 80-110 degrees C furnished mixture of products 4 and 5 in 28-68% yields. The chloro displacement with amines in compound 5 yielded 4-aminothieno[2,3-d]pyrimidine-6-carbonitrile derivatives 8(a h) and 9(a e). Antimicrobial activity of new compounds was studied against several bacteria such as Staphylococcus aureus MTCC-96, Escherichia coli MTCC-443, Pseudomonas aeruginosa MTCC-4 41, Streptococcus pyogenes MTCC-442 and fungi Aspergillus niger MTCC-282, Aspergillus clavatus MTCC-1323, Candida albicans MTCC-227 using broth microdilution method. Compounds 4, 8b, 8d, 8e, 8h and 9a showed promising antibacterial activity compared to ampicillin and compounds 8b, 8h showed better antifungal activity compared to greseofulvin. (C) 2013 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2013.03.039
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文献信息

  • Synthetic tactics of new class of 4-aminothieno[2,3-d]pyrimidine-6-carbonitrile derivatives acting as antimicrobial agents
    作者:Shrikant B. Kanawade、Raghunath B. Toche、Dhanji P. Rajani
    DOI:10.1016/j.ejmech.2013.03.039
    日期:2013.6
    Thermal selective reactions were studied on oxothieno[2,3-d]pyrimidine-6-carboxamide 3 with POCI3 and PCI5. At 25-50 degrees C, the C-7-amide rearranges to nitrile furnished compound 4 in 85-90% yield, while at 80-110 degrees C furnished mixture of products 4 and 5 in 28-68% yields. The chloro displacement with amines in compound 5 yielded 4-aminothieno[2,3-d]pyrimidine-6-carbonitrile derivatives 8(a h) and 9(a e). Antimicrobial activity of new compounds was studied against several bacteria such as Staphylococcus aureus MTCC-96, Escherichia coli MTCC-443, Pseudomonas aeruginosa MTCC-4 41, Streptococcus pyogenes MTCC-442 and fungi Aspergillus niger MTCC-282, Aspergillus clavatus MTCC-1323, Candida albicans MTCC-227 using broth microdilution method. Compounds 4, 8b, 8d, 8e, 8h and 9a showed promising antibacterial activity compared to ampicillin and compounds 8b, 8h showed better antifungal activity compared to greseofulvin. (C) 2013 Elsevier Masson SAS. All rights reserved.
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