Technology Process of C29H26F3N5O
There total 5 articles about C29H26F3N5O 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
benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
DOI:10.1021/jm301824k
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: sodium hydroxide / methanol / 6 h / 50 °C
1.2: pH 4
2.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dichloromethane
With
benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; sodium hydroxide;
In
methanol; dichloromethane;
DOI:10.1021/jm301824k
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / ethyl acetate / 20 °C / Inert atmosphere
2.1: potassium carbonate; methanol / 0.08 h / 20 °C
3.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 80 °C / Inert atmosphere
4.1: sodium hydroxide / methanol / 6 h / 50 °C
4.2: pH 4
5.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dichloromethane
With
methanol; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide;
In
1-methyl-pyrrolidin-2-one; methanol; dichloromethane; ethyl acetate;
1.1: |Sonogashira Cross-Coupling / 3.1: |Sonogashira Cross-Coupling;
DOI:10.1021/jm301824k