Technology Process of N-(2-(2-(5-amino-2-(4-chloro-1H-imidazol-1-yl)phenoxy)ethoxy)ethyl)-2-chloro-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine
There total 14 articles about N-(2-(2-(5-amino-2-(4-chloro-1H-imidazol-1-yl)phenoxy)ethoxy)ethyl)-2-chloro-7-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine 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: boron tribromide / dichloromethane / -78 - 4 °C / Inert atmosphere
2: caesium carbonate / tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 18 h / 20 °C
3: potassium hydroxide / dimethyl sulfoxide / 18 h / 90 °C
4: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 3 h / 20 °C
5: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 20 °C
6: ammonium chloride; iron / methanol / 5 h / 65 °C
With
hydrogenchloride; boron tribromide; iron; ammonium chloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; potassium hydroxide;
tetra-(n-butyl)ammonium iodide;
In
tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 5 steps
1: caesium carbonate / tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 18 h / 20 °C
2: potassium hydroxide / dimethyl sulfoxide / 18 h / 90 °C
3: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 3 h / 20 °C
4: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 20 °C
5: ammonium chloride; iron / methanol / 5 h / 65 °C
With
hydrogenchloride; iron; ammonium chloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; potassium hydroxide;
tetra-(n-butyl)ammonium iodide;
In
tetrahydrofuran; 1,4-dioxane; methanol; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: formic acid; dihydrogen peroxide / 4 h / 20 - 40 °C
2.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C
2.2: 3 h / 25 °C
3.1: potassium hydroxide / water / 20 °C
4.1: hydrogenchloride; water / 1 h / Reflux
5.1: ammonia / water / 5 h / Heating
6.1: trichlorophosphate / 1 h / 110 °C / microwave irradiation
7.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 20 °C
8.1: ammonium chloride; iron / methanol / 5 h / 65 °C
With
hydrogenchloride; n-butyllithium; formic acid; ammonia; water; dihydrogen peroxide; iron; ammonium chloride; diisopropylamine; N-ethyl-N,N-diisopropylamine; potassium hydroxide; trichlorophosphate;
In
tetrahydrofuran; methanol; hexanes; water; acetonitrile;