Technology Process of C13H12ClN3O4S
There total 6 articles about C13H12ClN3O4S which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
sodium tetrahydroborate;
In
ethanol;
for 0.5h;
- Guidance literature:
-
Multi-step reaction with 6 steps
1: pyridine / dichloromethane / 1.25 h / 20 °C / Cooling with ice; Inert atmosphere
2: 1,1'-azodicarbonyl-dipiperidine; triphenylphosphine / tetrahydrofuran / 3.25 h / 0 - 20 °C
3: potassium carbonate; ethanol / 1 h / Reflux
4: sodium hexamethyldisilazane / tetrahydrofuran / 1 h / 20 °C / Cooling with ice; Inert atmosphere
5: 3-chloro-benzenecarboperoxoic acid / chloroform / 0.25 h / Reflux
6: sodium tetrahydroborate / ethanol / 0.5 h
With
pyridine; sodium tetrahydroborate; ethanol; sodium hexamethyldisilazane; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine;
In
tetrahydrofuran; ethanol; dichloromethane; chloroform;
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1,1'-azodicarbonyl-dipiperidine; triphenylphosphine / tetrahydrofuran / 3.25 h / 0 - 20 °C
2: potassium carbonate; ethanol / 1 h / Reflux
3: sodium hexamethyldisilazane / tetrahydrofuran / 1 h / 20 °C / Cooling with ice; Inert atmosphere
4: 3-chloro-benzenecarboperoxoic acid / chloroform / 0.25 h / Reflux
5: sodium tetrahydroborate / ethanol / 0.5 h
With
sodium tetrahydroborate; ethanol; sodium hexamethyldisilazane; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine;
In
tetrahydrofuran; ethanol; chloroform;