Technology Process of C52H56N8O7S4
There total 16 articles about C52H56N8O7S4 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
benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;
In
dichloromethane;
at 0 - 20 ℃;
for 4.5h;
DOI:10.1002/anie.201302106
- Guidance literature:
-
Multi-step reaction with 2 steps
1: diethylamine / d7-N,N-dimethylformamide / 0.5 h / 20 °C
2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 4.5 h / 0 - 20 °C
With
benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; diethylamine;
In
dichloromethane; d7-N,N-dimethylformamide;
DOI:10.1002/anie.201302106
- Guidance literature:
-
Multi-step reaction with 6 steps
1: sulfuryl dichloride / dichloromethane / 1 h / 0 - 20 °C
2: ethanol / 40 °C
3: hydrogen; rosenmund catalyst / tetrahydrofuran; ethanol / 30 °C
4: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 4.5 h / 0 - 20 °C
5: diethylamine / d7-N,N-dimethylformamide / 0.5 h / 20 °C
6: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 4.5 h / 0 - 20 °C
With
sulfuryl dichloride; rosenmund catalyst; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; diethylamine;
In
tetrahydrofuran; ethanol; dichloromethane; d7-N,N-dimethylformamide;
DOI:10.1002/anie.201302106