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ethyl 4-(2-(2,2-dicyanovinyl)-4-nitro-5-(vinylthio)thien-3-yl)piperazine-1-carboxylate | 1449017-64-4

中文名称
——
中文别名
——
英文名称
ethyl 4-(2-(2,2-dicyanovinyl)-4-nitro-5-(vinylthio)thien-3-yl)piperazine-1-carboxylate
英文别名
Ethyl 4-[2-(2,2-dicyanoethenyl)-5-ethenylsulfanyl-4-nitrothiophen-3-yl]piperazine-1-carboxylate;ethyl 4-[2-(2,2-dicyanoethenyl)-5-ethenylsulfanyl-4-nitrothiophen-3-yl]piperazine-1-carboxylate
ethyl 4-(2-(2,2-dicyanovinyl)-4-nitro-5-(vinylthio)thien-3-yl)piperazine-1-carboxylate化学式
CAS
1449017-64-4
化学式
C17H17N5O4S2
mdl
——
分子量
419.485
InChiKey
YTQINGNSRMRWGP-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:
    28
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    180
  • 氢给体数:
    0
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    ethyl 4-(2-(2,2-dicyanovinyl)-4-nitro-5-(vinylthio)thien-3-yl)piperazine-1-carboxylate5,5-二甲基-1,3-环己二酮吗啉 作用下, 以 乙醇 为溶剂, 反应 11.0h, 以75%的产率得到ethyl 4-(2-(2-amino-3-cyano-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-4H-chromen-4-yl)-4-nitro-5-(vinylthio)thien-3-yl)piperazine-1-carboxylate
    参考文献:
    名称:
    Chemistry of Polyhalogenated Nitrobutadienes, 12: Synthesis of Novel, Highly Substituted Bi- and Tricyclic 5,6,7,8-Tetrahydro-4H-chromen-5-ones
    摘要:
    Knoevenagel condensation of 3,4-push-pull-substituted thiophene-2-carbaldehydes 4 with malononitrile gives the gem-dicyanovinylthiophenes 5, followed by a Michael addition of dimedone and a subsequent cyclization to 4-(2-thienyl)-5,6,7,8-tetrahydro-4H-chromen-5-ones 6. Protonolysis of the latter in methanol led to a mixture of four heterocycles 7-10, the main product being the novel tricyclic 9-(2-thienyl)-6,7-dihydro-5H-thieno[3,2-b]chromen-8(9H)-one derivative 7. A mechanism of the protonolysis reaction is proposed, the structures of the two products 7a/8a have been confirmed by X-ray analysis.
    DOI:
    10.3987/com-12-s(n)108
  • 作为产物:
    参考文献:
    名称:
    Chemistry of Polyhalogenated Nitrobutadienes, 12: Synthesis of Novel, Highly Substituted Bi- and Tricyclic 5,6,7,8-Tetrahydro-4H-chromen-5-ones
    摘要:
    Knoevenagel condensation of 3,4-push-pull-substituted thiophene-2-carbaldehydes 4 with malononitrile gives the gem-dicyanovinylthiophenes 5, followed by a Michael addition of dimedone and a subsequent cyclization to 4-(2-thienyl)-5,6,7,8-tetrahydro-4H-chromen-5-ones 6. Protonolysis of the latter in methanol led to a mixture of four heterocycles 7-10, the main product being the novel tricyclic 9-(2-thienyl)-6,7-dihydro-5H-thieno[3,2-b]chromen-8(9H)-one derivative 7. A mechanism of the protonolysis reaction is proposed, the structures of the two products 7a/8a have been confirmed by X-ray analysis.
    DOI:
    10.3987/com-12-s(n)108
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文献信息

  • Chemistry of Polyhalogenated Nitrobutadienes, 12: Synthesis of Novel, Highly Substituted Bi- and Tricyclic 5,6,7,8-Tetrahydro-4H-chromen-5-ones
    作者:Dieter E. Kaufmann、Viktor A. Zapol'skii、Eva-Janina Vogt、Mimoza Gjikaj
    DOI:10.3987/com-12-s(n)108
    日期:——
    Knoevenagel condensation of 3,4-push-pull-substituted thiophene-2-carbaldehydes 4 with malononitrile gives the gem-dicyanovinylthiophenes 5, followed by a Michael addition of dimedone and a subsequent cyclization to 4-(2-thienyl)-5,6,7,8-tetrahydro-4H-chromen-5-ones 6. Protonolysis of the latter in methanol led to a mixture of four heterocycles 7-10, the main product being the novel tricyclic 9-(2-thienyl)-6,7-dihydro-5H-thieno[3,2-b]chromen-8(9H)-one derivative 7. A mechanism of the protonolysis reaction is proposed, the structures of the two products 7a/8a have been confirmed by X-ray analysis.
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