Technology Process of C33H25BF2N2O5
There total 6 articles about C33H25BF2N2O5 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
potassium carbonate;
In
tetrahydrofuran; methanol; water;
at 25 ℃;
for 24h;
DOI:10.1016/j.bmcl.2011.01.040
- Guidance literature:
-
Multi-step reaction with 3 steps
1: boron trifluoride diethyl etherate; triethylamine / 1,2-dichloro-ethane / Inert atmosphere; Reflux
2: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / dichloromethane / 24 h / 25 °C / Inert atmosphere
3: potassium carbonate / tetrahydrofuran; methanol; water / 24 h / 25 °C
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; boron trifluoride diethyl etherate; potassium carbonate; triethylamine;
In
tetrahydrofuran; methanol; dichloromethane; water; 1,2-dichloro-ethane;
2: Sonogashira coupling;
DOI:10.1016/j.bmcl.2011.01.040
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: trifluoroacetic acid / dichloromethane / 1 h / 25 °C / Inert atmosphere
1.2: 0.5 h / Inert atmosphere
2.1: boron trifluoride diethyl etherate; triethylamine / 1,2-dichloro-ethane / Inert atmosphere; Reflux
3.1: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; triethylamine / dichloromethane / 24 h / 25 °C / Inert atmosphere
4.1: potassium carbonate / tetrahydrofuran; methanol; water / 24 h / 25 °C
With
bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; boron trifluoride diethyl etherate; potassium carbonate; triethylamine; trifluoroacetic acid;
In
tetrahydrofuran; methanol; dichloromethane; water; 1,2-dichloro-ethane;
3.1: Sonogashira coupling;
DOI:10.1016/j.bmcl.2011.01.040