Technology Process of C22H19F3N6O
There total 7 articles about C22H19F3N6O which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
Multi-step reaction with 6 steps
1: dimethyl sulfoxide / 150 °C
2: N-Bromosuccinimide / acetonitrile / 0 - 20 °C
3: tetrakis(triphenylphosphine) palladium(0); sodium carbonate / 1,4-dioxane; water / Reflux; Inert atmosphere
4: trifluoroacetic acid / dichloromethane
5: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 20 °C
6: trifluoroacetic acid / dichloromethane
With
N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium(0); sodium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid;
In
1,4-dioxane; dichloromethane; water; dimethyl sulfoxide; acetonitrile;
3: Suzuky-Miyaura coupling;
DOI:10.1016/j.bmcl.2011.01.086
- Guidance literature:
-
Multi-step reaction with 4 steps
1: tetrakis(triphenylphosphine) palladium(0); sodium carbonate / 1,4-dioxane; water / Reflux; Inert atmosphere
2: trifluoroacetic acid / dichloromethane
3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 20 °C
4: trifluoroacetic acid / dichloromethane
With
tetrakis(triphenylphosphine) palladium(0); sodium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid;
In
1,4-dioxane; dichloromethane; water;
1: Suzuky-Miyaura coupling;
DOI:10.1016/j.bmcl.2011.01.086
- Guidance literature:
-
Multi-step reaction with 3 steps
1: trifluoroacetic acid / dichloromethane
2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 20 °C
3: trifluoroacetic acid / dichloromethane
With
benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid;
In
dichloromethane;
DOI:10.1016/j.bmcl.2011.01.086