Technology Process of N-{1-[4-(5,7-dimethoxy-4-oxo-3,4-dihydroquinazolin-2-yl)phenyl]piperidin-4-yl}-N-ethylacetamide
There total 12 articles about N-{1-[4-(5,7-dimethoxy-4-oxo-3,4-dihydroquinazolin-2-yl)phenyl]piperidin-4-yl}-N-ethylacetamide 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
toluene-4-sulfonic acid; sodium hydrogensulfite;
In
N,N-dimethyl acetamide;
at 150 ℃;
for 4h;
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: dimethyl sulfoxide / 48 h / 120 °C / Inert atmosphere
2.1: triethylamine / dichloromethane / 0.08 h / Inert atmosphere
3.1: sodium azide / N,N-dimethyl-formamide / 5 h / 80 °C
4.1: acetic acid; palladium 10% on activated carbon; hydrogen / 1,4-dioxane; water / 5 h / 760.05 Torr
5.1: triethylamine / dichloromethane / 0.08 h / 20 °C
6.1: diisobutylaluminium hydride / dichloromethane; hexane / 1.33 h / -78 - 20 °C / Inert atmosphere
7.1: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / dichloromethane / 19 h / 20 °C / Molecular sieve
8.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.58 h / 0 °C
8.2: 2 h / 0 - 20 °C
9.1: sodium hydrogensulfite; toluene-4-sulfonic acid / N,N-dimethyl acetamide / 4 h / 150 °C
With
sodium azide; tetrapropylammonium perruthennate; palladium 10% on activated carbon; hydrogen; sodium hydride; diisobutylaluminium hydride; toluene-4-sulfonic acid; sodium hydrogensulfite; acetic acid; 4-methylmorpholine N-oxide; triethylamine;
In
1,4-dioxane; hexane; dichloromethane; N,N-dimethyl acetamide; water; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: dimethyl sulfoxide / 48 h / 120 °C / Inert atmosphere
2.1: triethylamine / dichloromethane / 0.08 h / Inert atmosphere
3.1: sodium azide / N,N-dimethyl-formamide / 5 h / 80 °C
4.1: acetic acid; palladium 10% on activated carbon; hydrogen / 1,4-dioxane; water / 5 h / 760.05 Torr
5.1: triethylamine / dichloromethane / 0.08 h / 20 °C
6.1: diisobutylaluminium hydride / dichloromethane; hexane / 1.33 h / -78 - 20 °C / Inert atmosphere
7.1: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / dichloromethane / 19 h / 20 °C / Molecular sieve
8.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.58 h / 0 °C
8.2: 2 h / 0 - 20 °C
9.1: sodium hydrogensulfite; toluene-4-sulfonic acid / N,N-dimethyl acetamide / 4 h / 150 °C
With
sodium azide; tetrapropylammonium perruthennate; palladium 10% on activated carbon; hydrogen; sodium hydride; diisobutylaluminium hydride; toluene-4-sulfonic acid; sodium hydrogensulfite; acetic acid; 4-methylmorpholine N-oxide; triethylamine;
In
1,4-dioxane; hexane; dichloromethane; N,N-dimethyl acetamide; water; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;