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2-[5'-(4-cyanophenyl)-2,2'-bithiophen-5-yl]-1H-benzimidazole-6-carbonitrile | 1268709-37-0

中文名称
——
中文别名
——
英文名称
2-[5'-(4-cyanophenyl)-2,2'-bithiophen-5-yl]-1H-benzimidazole-6-carbonitrile
英文别名
2-[5-[5-(4-cyanophenyl)thiophen-2-yl]thiophen-2-yl]-3H-benzimidazole-5-carbonitrile
2-[5'-(4-cyanophenyl)-2,2'-bithiophen-5-yl]-1H-benzimidazole-6-carbonitrile化学式
CAS
1268709-37-0
化学式
C23H12N4S2
mdl
——
分子量
408.507
InChiKey
DAHLKPJJZRUBJP-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):
    5.3
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    133
  • 氢给体数:
    1
  • 氢受体数:
    5

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:
    Synthesis of Novel Bithiophene-Substituted Heterocycles Bearing Carbonitrile Groups
    摘要:
    Symmetrical and unsymmetrical bithiophene-substituted heterocycles bearing carbonitriles including imidazo[1,2-a]pyridine, benzimidazole, and pyridine derivatives have been synthesized via different synthetic protocols. The bithiophene bis-imidazo[1,2-a] pyridine derivatives 3a,b were achieved in three steps starting from 2-acetyl-5-bromothiophene. Suzuki coupling reaction of 2a with 5-formylthiophen-2-ylboronic acid forms the formyl derivative 5, which by condensation with 3,4-diaminobenzonitrile in the presence of sodium bisulfite furnishes the unsymmetrical bithiophene derivative6. The bis-benzimidazole derivative 8 was obtained via hexabutylditin-mediated homocoupling of 5-bromothiophene-2-carboxaldehyde, while the benzimidazole derivatives 12a,b were prepared via the formyl derivatives 11a,b, a product of Velsmier formylation reaction of 10a,b. Two synthetic protocols for the aryl/hetaryl-2,2'-bithiophene derivative 14 have also been presented. In addition, the guanyl hydrazones of bithiophenes, 16 and 17, were prepared from bis(tri-n-butylstannyl)-2,2'-bithiophene through a Stille coupling reaction followed by a condensation step.
    DOI:
    10.1080/00397910903537364
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