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3-(2-(2-aminopyrimidin-5-yl)ethynyl)-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide

Base Information Edit
  • Chemical Name:3-(2-(2-aminopyrimidin-5-yl)ethynyl)-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide
  • CAS No.:1257628-82-2
  • Molecular Formula:C25H19F3N6O
  • Molecular Weight:476.461
  • Hs Code.:
  • Mol file:1257628-82-2.mol
3-(2-(2-aminopyrimidin-5-yl)ethynyl)-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide

Synonyms:3-(2-(2-aminopyrimidin-5-yl)ethynyl)-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide

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Chemical Property of 3-(2-(2-aminopyrimidin-5-yl)ethynyl)-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide Edit
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Technology Process of 3-(2-(2-aminopyrimidin-5-yl)ethynyl)-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide

There total 5 articles about 3-(2-(2-aminopyrimidin-5-yl)ethynyl)-4-methyl-N-(3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide 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:
With copper(l) iodide; palladium diacetate; N-ethyl-N,N-diisopropylamine; tricyclohexylphosphine; In N,N-dimethyl-formamide; at 60 ℃; Sealed tube; Inert atmosphere;
DOI:10.1016/j.bmcl.2015.07.006
Guidance literature:
Multi-step reaction with 4 steps
1.1: thionyl chloride / N,N-dimethyl-formamide / 2 h / Reflux
2.1: triethylamine / tetrahydrofuran / 1 h / 0 - 20 °C
3.1: palladium bis[bis(diphenylphosphino)ferrocene] dichloride; triethylamine; copper(l) iodide / acetonitrile / 2 h / 80 °C / Sealed tube; Inert atmosphere
3.2: 3 h / 20 °C
4.1: palladium diacetate; tricyclohexylphosphine; N-ethyl-N,N-diisopropylamine; copper(l) iodide / N,N-dimethyl-formamide / 60 °C / Sealed tube; Inert atmosphere
With copper(l) iodide; thionyl chloride; palladium bis[bis(diphenylphosphino)ferrocene] dichloride; palladium diacetate; triethylamine; N-ethyl-N,N-diisopropylamine; tricyclohexylphosphine; In tetrahydrofuran; N,N-dimethyl-formamide; acetonitrile; 3.1: |Sonogashira Cross-Coupling / 4.1: |Sonogashira Cross-Coupling;
DOI:10.1016/j.bmcl.2015.07.006
Guidance literature:
Multi-step reaction with 3 steps
1.1: triethylamine / tetrahydrofuran / 1 h / 0 - 20 °C
2.1: palladium bis[bis(diphenylphosphino)ferrocene] dichloride; triethylamine; copper(l) iodide / acetonitrile / 2 h / 80 °C / Sealed tube; Inert atmosphere
2.2: 3 h / 20 °C
3.1: palladium diacetate; tricyclohexylphosphine; N-ethyl-N,N-diisopropylamine; copper(l) iodide / N,N-dimethyl-formamide / 60 °C / Sealed tube; Inert atmosphere
With copper(l) iodide; palladium bis[bis(diphenylphosphino)ferrocene] dichloride; palladium diacetate; triethylamine; N-ethyl-N,N-diisopropylamine; tricyclohexylphosphine; In tetrahydrofuran; N,N-dimethyl-formamide; acetonitrile; 2.1: |Sonogashira Cross-Coupling / 3.1: |Sonogashira Cross-Coupling;
DOI:10.1016/j.bmcl.2015.07.006
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