Technology Process of C59H77I2NO
There total 8 articles about C59H77I2NO 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 6 steps
1: sodium azide / N,N-dimethyl-formamide / 3 h / 70 °C / Inert atmosphere
2: tin(ll) chloride / methanol / 4 h / 0 - 20 °C
3: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane
4: triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / tetrahydrofuran / 20 °C / Inert atmosphere
5: potassium hydroxide / methanol; tetrahydrofuran
6: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; N-ethyl-N,N-diisopropylamine / tetrahydrofuran
With
dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; sodium azide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; tin(ll) chloride; potassium hydroxide;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
4: |Sonogashira Cross-Coupling / 6: |Sonogashira Cross-Coupling;
DOI:10.1021/ja3116422
- Guidance literature:
-
Multi-step reaction with 7 steps
1: dmap; triethylamine / dichloromethane / 2 h
2: sodium azide / N,N-dimethyl-formamide / 3 h / 70 °C / Inert atmosphere
3: tin(ll) chloride / methanol / 4 h / 0 - 20 °C
4: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane
5: triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / tetrahydrofuran / 20 °C / Inert atmosphere
6: potassium hydroxide / methanol; tetrahydrofuran
7: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; N-ethyl-N,N-diisopropylamine / tetrahydrofuran
With
dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; sodium azide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; tin(ll) chloride; potassium hydroxide;
In
tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
5: |Sonogashira Cross-Coupling / 7: |Sonogashira Cross-Coupling;
DOI:10.1021/ja3116422
- Guidance literature:
-
Multi-step reaction with 5 steps
1: tin(ll) chloride / methanol / 4 h / 0 - 20 °C
2: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane
3: triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide / tetrahydrofuran / 20 °C / Inert atmosphere
4: potassium hydroxide / methanol; tetrahydrofuran
5: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; N-ethyl-N,N-diisopropylamine / tetrahydrofuran
With
dmap; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; tin(ll) chloride; potassium hydroxide;
In
tetrahydrofuran; methanol; dichloromethane;
3: |Sonogashira Cross-Coupling / 5: |Sonogashira Cross-Coupling;
DOI:10.1021/ja3116422