Technology Process of C15H16N2O8
There total 1 articles about C15H16N2O8 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; trichloroisocyanuric acid;
In
dichloromethane;
at 0 ℃;
- Guidance literature:
-
With
2,6-dimethylpyridine;
In
dichloromethane;
at -45 - 40 ℃;
for 1h;
Inert atmosphere;
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: 2,6-dimethylpyridine / dichloromethane / 1 h / -45 - 40 °C / Inert atmosphere
2.1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / toluene; ethanol; water / Inert atmosphere
3.1: lithium borohydride; ethanol / tetrahydrofuran / 1 h / 15 - 25 °C / Cooling with ice
4.1: zinc; acetic acid / ethanol / 0.08 h / Reflux
5.1: triethylamine / tetrahydrofuran / 0.17 h / 0 °C
5.2: 20 - 65 °C
6.1: potassium carbonate / water; methanol / 0.83 h / 20 °C
7.1: Dess-Martin periodane / dichloromethane / 6.5 h / 20 °C
8.1: pyrrolidine / tetrakis(triphenylphosphine) palladium(0) / dichloromethane / 0.75 h / 20 °C / Inert atmosphere
9.1: N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline / dichloromethane; methanol / 24 h / 20 °C
With
pyrrolidine; 2,6-dimethylpyridine; lithium borohydride; ethanol; sodium carbonate; potassium carbonate; Dess-Martin periodane; acetic acid; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; triethylamine; zinc;
tetrakis(triphenylphosphine) palladium(0);
In
tetrahydrofuran; methanol; ethanol; dichloromethane; water; toluene;
2.1: Suzuki Coupling;