Technology Process of C14H10F3N5
There total 6 articles about C14H10F3N5 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
trimethylaluminum; ammonium chloride;
In
toluene;
at 110 ℃;
for 3h;
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 0.5 h / 20 °C
2: hydrogenchloride; hydrogen / palladium on activated charcoal / water; methanol / 2 h / 2068.65 Torr
3: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 18 h / 20 °C
4: trichlorophosphate / 1,2-dichloro-ethane / 3 h / Reflux
5: N-iodo-succinimide / acetonitrile / 0.33 h / Reflux
6: 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0) / N,N-dimethyl-formamide; water / 1 h / 110 °C
7: ammonium chloride; trimethylaluminum / toluene / 3 h / 110 °C
With
hydrogenchloride; N-iodo-succinimide; hydrogen; trimethylaluminum; ammonium chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trichlorophosphate;
1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0); palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 4 steps
1: trichlorophosphate / 1,2-dichloro-ethane / 3 h / Reflux
2: N-iodo-succinimide / acetonitrile / 0.33 h / Reflux
3: 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0) / N,N-dimethyl-formamide; water / 1 h / 110 °C
4: ammonium chloride; trimethylaluminum / toluene / 3 h / 110 °C
With
N-iodo-succinimide; trimethylaluminum; ammonium chloride; trichlorophosphate;
1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0);
In
water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene; acetonitrile;