Technology Process of 1,2-dimethyl-3-phenylquinolin-4(1H)-one
There total 6 articles about 1,2-dimethyl-3-phenylquinolin-4(1H)-one 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
dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0);
In
toluene;
at 80 ℃;
for 0.75h;
Inert atmosphere;
DOI:10.1021/jo1014504
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: caesium carbonate / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere
1.2: 20 °C / Inert atmosphere
2.1: dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; tris-(dibenzylideneacetone)dipalladium(0); potassium phosphate / toluene / 0.75 h / 80 °C / Inert atmosphere
With
dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate;
In
N,N-dimethyl-formamide; toluene;
2.1: Suzuki-Miyaura coupling;
DOI:10.1021/jo1014504
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: iodine; potassium iodide; sodium hydroxide / water / 20 °C / Inert atmosphere
2.1: caesium carbonate / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere
2.2: 20 °C / Inert atmosphere
3.1: dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; tris-(dibenzylideneacetone)dipalladium(0); potassium phosphate / toluene / 0.75 h / 80 °C / Inert atmosphere
With
dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); iodine; caesium carbonate; potassium iodide; sodium hydroxide;
In
water; N,N-dimethyl-formamide; toluene;
3.1: Suzuki-Miyaura coupling;
DOI:10.1021/jo1014504
