Technology Process of C23H27N5O5
There total 8 articles about C23H27N5O5 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
trifluoroacetic acid;
In
dichloromethane;
at 20 ℃;
for 20h;
- Guidance literature:
-
Multi-step reaction with 5 steps
1: hydrogen / palladium on activated charcoal / tetrahydrofuran; thiophene; di-isopropyl ether / 20 h / 20 °C
2: toluene-4-sulfonic acid / 1,4-dioxane / 20 h / 100 °C
3: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 °C
4: N-ethyl-N,N-diisopropylamine / acetonitrile / 72 h / 70 °C
5: trifluoroacetic acid / dichloromethane / 20 h / 20 °C
With
hydrogen; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid;
palladium on activated charcoal;
In
tetrahydrofuran; 1,4-dioxane; thiophene; dichloromethane; di-isopropyl ether; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 7 steps
1: hydrazine hydrate / ethanol / 1 h / 50 °C
2: triethylamine / 1,4-dioxane / 20 °C
3: hydrogen / palladium on activated charcoal / tetrahydrofuran; thiophene; di-isopropyl ether / 20 h / 20 °C
4: toluene-4-sulfonic acid / 1,4-dioxane / 20 h / 100 °C
5: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 °C
6: N-ethyl-N,N-diisopropylamine / acetonitrile / 72 h / 70 °C
7: trifluoroacetic acid / dichloromethane / 20 h / 20 °C
With
hydrogen; toluene-4-sulfonic acid; hydrazine hydrate; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid;
palladium on activated charcoal;
In
tetrahydrofuran; 1,4-dioxane; thiophene; ethanol; dichloromethane; di-isopropyl ether; acetonitrile;