Technology Process of C53H62N6O13
There total 15 articles about C53H62N6O13 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
Dess-Martin periodane;
In
dichloromethane;
at 20 ℃;
for 6.5h;
- Guidance literature:
-
With
Dess-Martin periodane;
In
dichloromethane;
at 20 ℃;
for 6.5h;
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: trichloroisocyanuric acid; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / dichloromethane / 0 °C
2.1: 2,6-dimethylpyridine / dichloromethane / 1 h / -45 - 40 °C / Inert atmosphere
3.1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / toluene; ethanol; water / Inert atmosphere
4.1: lithium borohydride; ethanol / tetrahydrofuran / 1 h / 15 - 25 °C / Cooling with ice
5.1: zinc; acetic acid / ethanol / 0.08 h / Reflux
6.1: triethylamine / tetrahydrofuran / 0.17 h / 0 °C
6.2: 20 - 65 °C
7.1: potassium carbonate / water; methanol / 0.83 h / 20 °C
8.1: Dess-Martin periodane / dichloromethane / 6.5 h / 20 °C
With
2,6-dimethylpyridine; lithium borohydride; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; ethanol; trichloroisocyanuric acid; sodium carbonate; potassium carbonate; Dess-Martin periodane; acetic acid; triethylamine; zinc;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran; methanol; ethanol; dichloromethane; water; toluene;
3.1: Suzuki Coupling;