Technology Process of C17H13ClN4OS
There total 7 articles about C17H13ClN4OS which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
ammonia;
In
isopropyl alcohol;
at 50 ℃;
for 0.5h;
- Guidance literature:
-
Multi-step reaction with 7 steps
1: potassium carbonate; ethanol / 1 h / Reflux
2: sodium hexamethyldisilazane / tetrahydrofuran / 1 h / 20 °C / Cooling with ice; Inert atmosphere
3: hydrogen / palladium 10% on activated carbon / isopropyl alcohol / 6 h / 20 °C
4: sodium hydride / pyridine; oil / 3 h / 50 °C / Cooling with ice
5: triethylamine / copper diacetate / dichloromethane / 1 h / Reflux
6: 3-chloro-benzenecarboperoxoic acid / chloroform / 0.75 h / Reflux
7: ammonia / isopropyl alcohol / 0.5 h / 50 °C
With
ethanol; ammonia; hydrogen; sodium hexamethyldisilazane; sodium hydride; potassium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid;
palladium 10% on activated carbon; copper diacetate;
In
tetrahydrofuran; pyridine; dichloromethane; chloroform; isopropyl alcohol; oil;
- Guidance literature:
-
Multi-step reaction with 6 steps
1: sodium hexamethyldisilazane / tetrahydrofuran / 1 h / 20 °C / Cooling with ice; Inert atmosphere
2: hydrogen / palladium 10% on activated carbon / isopropyl alcohol / 6 h / 20 °C
3: sodium hydride / pyridine; oil / 3 h / 50 °C / Cooling with ice
4: triethylamine / copper diacetate / dichloromethane / 1 h / Reflux
5: 3-chloro-benzenecarboperoxoic acid / chloroform / 0.75 h / Reflux
6: ammonia / isopropyl alcohol / 0.5 h / 50 °C
With
ammonia; hydrogen; sodium hexamethyldisilazane; sodium hydride; triethylamine; 3-chloro-benzenecarboperoxoic acid;
palladium 10% on activated carbon; copper diacetate;
In
tetrahydrofuran; pyridine; dichloromethane; chloroform; isopropyl alcohol; oil;