Technology Process of 1-Piperazinecarboxylic acid,
3-methyl-6-[(1-methyl-1H-indol-3-yl)methyl]-2,5-dioxo-4-(phenylmethyl)-,
methyl ester, (3S,6S)-
There total 4 articles about 1-Piperazinecarboxylic acid,
3-methyl-6-[(1-methyl-1H-indol-3-yl)methyl]-2,5-dioxo-4-(phenylmethyl)-,
methyl ester, (3S,6S)- 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
dmap; triethylamine;
In
dichloromethane;
at 20 ℃;
for 20h;
DOI:10.1021/jo0342572
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 73 percent / Na2CO3 / H2O; dioxane / 20 h / 20 °C
2: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxy-7-azabenzotriazole / CH2Cl2 / 24 h / 20 °C
3: 250 mg / H2 / Pd/C / methanol / 20 °C
4: 40 percent / 4-dimethylaminopyridine; triethylamine / CH2Cl2 / 20 h / 20 °C
With
dmap; 1-hydroxy-7-aza-benzotriazole; hydrogen; sodium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine;
palladium on activated charcoal;
In
1,4-dioxane; methanol; dichloromethane; water;
DOI:10.1021/jo0342572
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-hydroxy-7-azabenzotriazole / CH2Cl2 / 24 h / 20 °C
2: 250 mg / H2 / Pd/C / methanol / 20 °C
3: 40 percent / 4-dimethylaminopyridine; triethylamine / CH2Cl2 / 20 h / 20 °C
With
dmap; 1-hydroxy-7-aza-benzotriazole; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine;
palladium on activated charcoal;
In
methanol; dichloromethane;
DOI:10.1021/jo0342572
