Technology Process of C23H22ClN3O3
There total 1 articles about C23H22ClN3O3 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:
-
6-acetamido-3-methyl-1,2-benzisoxazole;
With
lithium diisopropyl amide;
In
tetrahydrofuran;
at -78 ℃;
for 0.916667h;
Inert atmosphere;
4-chloromethyl-2-(2-chlorophenyl)-5-propyloxazole;
In
tetrahydrofuran;
at -78 - 20 ℃;
Inert atmosphere;
DOI:10.1016/j.bmc.2011.03.053
- Guidance literature:
-
C23H22ClN3O3;
With
hydrogenchloride; water; acetic acid;
for 24h;
Reflux;
With
sodium hydroxide;
In
water;
Cooling with ice;
DOI:10.1016/j.bmc.2011.03.053
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: hydrogenchloride; water; acetic acid / 24 h / Reflux
1.2: Cooling with ice
2.1: sulfuric acid; water; sodium nitrite / 3.33 h / 0 - 130 °C
3.1: potassium carbonate / butanone / 45 h / Reflux
4.1: lithium hydroxide monohydrate / ethanol; water / 2 h / Reflux
4.2: Cooling with ice
With
hydrogenchloride; lithium hydroxide monohydrate; sulfuric acid; water; potassium carbonate; acetic acid; sodium nitrite;
In
ethanol; water; butanone;
DOI:10.1016/j.bmc.2011.03.053