Technology Process of C32H34N4O8
There total 3 articles about C32H34N4O8 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:
-
5-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidine-1-carboxylic acid tert-butyl ester;
With
caesium carbonate;
In
acetonitrile;
at 20 ℃;
for 0.5h;
Inert atmosphere;
1,2-bis-(3-bromo-1-propynyl)benzene;
In
acetonitrile;
at 20 ℃;
for 6h;
Inert atmosphere;
DOI:10.1016/j.tet.2012.07.093
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: lithium bromide / tetrahydrofuran / 10 h / 0 - 20 °C / Inert atmosphere
2.1: caesium carbonate / acetonitrile / 0.5 h / 20 °C / Inert atmosphere
2.2: 6 h / 20 °C / Inert atmosphere
With
caesium carbonate; lithium bromide;
In
tetrahydrofuran; acetonitrile;
DOI:10.1016/j.tet.2012.07.093
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: tetrakis(triphenylphosphine) palladium(0); N-butylamine / 80 - 85 °C / Inert atmosphere
2.1: triethylamine / dichloromethane / 0.25 h / 0 °C / Inert atmosphere
3.1: lithium bromide / tetrahydrofuran / 10 h / 0 - 20 °C / Inert atmosphere
4.1: caesium carbonate / acetonitrile / 0.5 h / 20 °C / Inert atmosphere
4.2: 6 h / 20 °C / Inert atmosphere
With
tetrakis(triphenylphosphine) palladium(0); caesium carbonate; N-butylamine; triethylamine; lithium bromide;
In
tetrahydrofuran; dichloromethane; acetonitrile;
1.1: |Sonogashira Cross-Coupling;
DOI:10.1016/j.tet.2012.07.093