Technology Process of C12H17N3O2
There total 4 articles about C12H17N3O2 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:
-
With
hydrogenchloride; water;
In
1,4-dioxane; dichloromethane;
at 20 ℃;
for 5h;
DOI:10.1016/j.bmcl.2011.02.033
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 18-crown-6 ether; potassium carbonate / acetonitrile / 20 h / Reflux
2: palladium diacetate; caesium carbonate; XPhos / 1,4-dioxane / 20 h / Reflux
3: 5% Pd(II)/C(eggshell); hydrogen / 2 h / 20 °C
4: 18-crown-6 ether; potassium carbonate / acetonitrile / 20 h / Reflux
5: hydrogenchloride; water / 1,4-dioxane; dichloromethane / 5 h / 20 °C
With
hydrogenchloride; 18-crown-6 ether; 5% Pd(II)/C(eggshell); water; hydrogen; palladium diacetate; potassium carbonate; caesium carbonate; XPhos;
In
1,4-dioxane; dichloromethane; acetonitrile;
2: Buchwald amination;
DOI:10.1016/j.bmcl.2011.02.033
- Guidance literature:
-
Multi-step reaction with 2 steps
1: 18-crown-6 ether; potassium carbonate / acetonitrile / 20 h / Reflux
2: hydrogenchloride; water / 1,4-dioxane; dichloromethane / 5 h / 20 °C
With
hydrogenchloride; 18-crown-6 ether; water; potassium carbonate;
In
1,4-dioxane; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2011.02.033