Technology Process of C21H16ClF4N3O3
There total 14 articles about C21H16ClF4N3O3 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
thionyl chloride;
at 0 - 40 ℃;
for 4.5h;
Cooling with ice;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; triethylamine / dichloromethane / 23 °C / Cooling with ice
2: ethanol; sodium hydroxide / 4 h / 80 °C
3: thionyl chloride / 4.5 h / 0 - 40 °C / Cooling with ice
With
thionyl chloride; ethanol; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide;
In
dichloromethane;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: hydrogen; ammonia / methanol / 80 °C / 7500.75 Torr
2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; triethylamine / dichloromethane / 23 °C / Cooling with ice
3: ethanol; sodium hydroxide / 4 h / 80 °C
4: thionyl chloride / 4.5 h / 0 - 40 °C / Cooling with ice
With
thionyl chloride; ethanol; ammonia; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide;
In
methanol; dichloromethane;