Technology Process of C43H44ClN7O5S2
There total 7 articles about C43H44ClN7O5S2 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:
-
Multi-step reaction with 5 steps
1: hydroxylamine hydrochloride; sodium carbonate; acetic acid / methanol; water / 4 h / Reflux
2: L-proline; copper(l) iodide / dimethyl sulfoxide / 20 °C / Inert atmosphere
3: palladium 10% on activated carbon; hydrogen / methanol / 0.25 h / 760.05 Torr / Inert atmosphere
4: pyridine / 0.5 h / 0 °C
5: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide
With
pyridine; copper(l) iodide; palladium 10% on activated carbon; hydroxylamine hydrochloride; hydrogen; sodium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; L-proline;
In
methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
2: |Ullmann Condensation;
DOI:10.1021/jm4001105
- Guidance literature:
-
Multi-step reaction with 4 steps
1: L-proline; copper(l) iodide / dimethyl sulfoxide / 20 °C / Inert atmosphere
2: palladium 10% on activated carbon; hydrogen / methanol / 0.25 h / 760.05 Torr / Inert atmosphere
3: pyridine / 0.5 h / 0 °C
4: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide
With
pyridine; copper(l) iodide; palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; L-proline;
In
methanol; dimethyl sulfoxide; N,N-dimethyl-formamide;
1: |Ullmann Condensation;
DOI:10.1021/jm4001105
- Guidance literature:
-
Multi-step reaction with 2 steps
1: pyridine / 0.5 h / 0 °C
2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide
With
pyridine; N-ethyl-N,N-diisopropylamine;
In
N,N-dimethyl-formamide;
DOI:10.1021/jm4001105