Technology Process of 2-(2-chloro-4-(2,4-dibromophenyl)thiazol-5-ylthio)-N-o-tolylacetamide
There total 6 articles about 2-(2-chloro-4-(2,4-dibromophenyl)thiazol-5-ylthio)-N-o-tolylacetamide 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
tert.-butylnitrite; copper(l) chloride;
In
acetonitrile;
at 20 ℃;
for 0.25h;
Inert atmosphere;
DOI:10.1007/s12272-012-0604-y
- Guidance literature:
-
Multi-step reaction with 5 steps
1: ethanol / 20 °C
2: sodium hydroxide / dimethyl sulfoxide / 4 h / 20 °C
3: phosphorus pentachloride / diethyl ether / 5 h / 20 °C
4: triethylamine / dichloromethane / 10 h / 20 °C / Cooling with ice
5: tert.-butylnitrite; copper(l) chloride / acetonitrile / 0.25 h / 20 °C / Inert atmosphere
With
tert.-butylnitrite; phosphorus pentachloride; triethylamine; copper(l) chloride; sodium hydroxide;
In
diethyl ether; ethanol; dichloromethane; dimethyl sulfoxide; acetonitrile;
5: Sandmeyer reaction;
DOI:10.1007/s12272-012-0604-y
- Guidance literature:
-
Multi-step reaction with 8 steps
1: aluminum (III) chloride / 20 - 65 °C
2: sodium carbonate / ethanol / 12 h / 20 °C
3: bromine / acetic acid / 8.5 h / 20 °C
4: ethanol / 20 °C
5: sodium hydroxide / dimethyl sulfoxide / 4 h / 20 °C
6: phosphorus pentachloride / diethyl ether / 5 h / 20 °C
7: triethylamine / dichloromethane / 10 h / 20 °C / Cooling with ice
8: tert.-butylnitrite; copper(l) chloride / acetonitrile / 0.25 h / 20 °C / Inert atmosphere
With
aluminum (III) chloride; tert.-butylnitrite; phosphorus pentachloride; bromine; sodium carbonate; triethylamine; copper(l) chloride; sodium hydroxide;
In
diethyl ether; ethanol; dichloromethane; acetic acid; dimethyl sulfoxide; acetonitrile;
1: Friedel Crafts reaction / 8: Sandmeyer reaction;
DOI:10.1007/s12272-012-0604-y