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1-(1,2-dimethyl-7-azaindole-3-yl)-2-(2-methyl-5-phenyl-3-thienyl)perfluorocyclopentene

Base Information Edit
  • Chemical Name:1-(1,2-dimethyl-7-azaindole-3-yl)-2-(2-methyl-5-phenyl-3-thienyl)perfluorocyclopentene
  • CAS No.:1592848-00-4
  • Molecular Formula:C25H18F6N2S
  • Molecular Weight:492.488
  • Hs Code.:
  • Mol file:1592848-00-4.mol
1-(1,2-dimethyl-7-azaindole-3-yl)-2-(2-methyl-5-phenyl-3-thienyl)perfluorocyclopentene

Synonyms:1-(1,2-dimethyl-7-azaindole-3-yl)-2-(2-methyl-5-phenyl-3-thienyl)perfluorocyclopentene

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Chemical Property of 1-(1,2-dimethyl-7-azaindole-3-yl)-2-(2-methyl-5-phenyl-3-thienyl)perfluorocyclopentene Edit
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Technology Process of 1-(1,2-dimethyl-7-azaindole-3-yl)-2-(2-methyl-5-phenyl-3-thienyl)perfluorocyclopentene

There total 8 articles about 1-(1,2-dimethyl-7-azaindole-3-yl)-2-(2-methyl-5-phenyl-3-thienyl)perfluorocyclopentene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
1,2-dimethyl-3-bromine-7-azaindole; With n-butyllithium; In tetrahydrofuran; hexane; at -78.16 ℃; for 0.5h; Inert atmosphere;
1-[2-methyl-5-phenyl-3-thienyl]heptafluorocyclopentene; In tetrahydrofuran; hexane; at -78.16 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.dyepig.2014.03.003
Guidance literature:
Multi-step reaction with 5 steps
1.1: N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide / dichloromethane / 0.17 h / -0.16 °C
1.2: 12.33 h / 0 - 20 °C
2.1: lithium diisopropyl amide / hexane; tetrahydrofuran / 0.5 h / -25.16 °C / Inert atmosphere
2.2: 10 h / 20 - 25 °C / Inert atmosphere
3.1: N-Bromosuccinimide; tetrachloromethane / 12 h / 20 °C
4.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / -0.16 °C
4.2: 24 h / -0.16 °C
5.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / -78.16 °C / Inert atmosphere
5.2: 2 h / -78.16 °C / Inert atmosphere
With tetrachloromethane; N-Bromosuccinimide; n-butyllithium; N-benzyl-N,N,N-triethylammonium chloride; sodium hydride; sodium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.dyepig.2014.03.003
Guidance literature:
Multi-step reaction with 4 steps
1.1: lithium diisopropyl amide / hexane; tetrahydrofuran / 0.5 h / -25.16 °C / Inert atmosphere
1.2: 10 h / 20 - 25 °C / Inert atmosphere
2.1: N-Bromosuccinimide; tetrachloromethane / 12 h / 20 °C
3.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / -0.16 °C
3.2: 24 h / -0.16 °C
4.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / -78.16 °C / Inert atmosphere
4.2: 2 h / -78.16 °C / Inert atmosphere
With tetrachloromethane; N-Bromosuccinimide; n-butyllithium; sodium hydride; lithium diisopropyl amide; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1016/j.dyepig.2014.03.003
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