Technology Process of (3,4-Diamino-5-methyl-phenyl)-thiophen-2-yl-methanone
There total 7 articles about (3,4-Diamino-5-methyl-phenyl)-thiophen-2-yl-methanone 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
hydrogen;
palladium on activated charcoal;
In
methanol;
at 50 ℃;
for 2h;
DOI:10.1021/jm00122a020
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 99 percent / AlCl3 / CH2Cl2 / 0.75 h / < 12 deg C
2: 95 percent / BBr3 / CH2Cl2 / a) ice cooling, 30 min, b) room temperature, 5 h
3: 96 percent / conc. sulfuric acid, conc. nitric acid / 2 h / ice cooling
4: 47 percent / K2CO3 / acetone / 12 h / Heating
5: 98 percent / ammonia (g) / dimethylsulfoxide / 3 h / 85 °C
6: H2 / 10percent Pd/C / methanol / 2 h / 50 °C
With
aluminium trichloride; sulfuric acid; ammonia; hydrogen; nitric acid; boron tribromide; potassium carbonate;
palladium on activated charcoal;
In
methanol; dichloromethane; dimethyl sulfoxide; acetone;
DOI:10.1021/jm00122a020
- Guidance literature:
-
Multi-step reaction with 7 steps
1: thionyl chloride / CHCl3 / Heating
2: 99 percent / AlCl3 / CH2Cl2 / 0.75 h / < 12 deg C
3: 95 percent / BBr3 / CH2Cl2 / a) ice cooling, 30 min, b) room temperature, 5 h
4: 96 percent / conc. sulfuric acid, conc. nitric acid / 2 h / ice cooling
5: 47 percent / K2CO3 / acetone / 12 h / Heating
6: 98 percent / ammonia (g) / dimethylsulfoxide / 3 h / 85 °C
7: H2 / 10percent Pd/C / methanol / 2 h / 50 °C
With
aluminium trichloride; thionyl chloride; sulfuric acid; ammonia; hydrogen; nitric acid; boron tribromide; potassium carbonate;
palladium on activated charcoal;
In
methanol; dichloromethane; chloroform; dimethyl sulfoxide; acetone;
DOI:10.1021/jm00122a020