Technology Process of 5-[(3S,7S)-3,7-dimethyl-1-tetradecanesulfonyl]-1-phenyl-1H-tetrazole
There total 13 articles about 5-[(3S,7S)-3,7-dimethyl-1-tetradecanesulfonyl]-1-phenyl-1H-tetrazole 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
3-chloro-benzenecarboperoxoic acid;
In
dichloromethane;
at 0 - 20 ℃;
DOI:10.1021/jo4006602
- Guidance literature:
-
Multi-step reaction with 2 steps
1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere
2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C
With
3-chloro-benzenecarboperoxoic acid; triphenylphosphine; diethylazodicarboxylate;
In
tetrahydrofuran; dichloromethane;
DOI:10.1021/jo4006602
- Guidance literature:
-
Multi-step reaction with 7 steps
1: hydrazine; copper(II) sulfate; oxygen / ethanol / 15 h / 70 °C
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C
3: dmap / perdeuteriopyridine / 0 - 20 °C / Inert atmosphere
4: copper(I) bromide dimethylsulfide complex / tetrahydrofuran; diethyl ether / -78 - 0 °C / Inert atmosphere
5: hydrogen; palladium 10% on activated carbon / ethyl acetate / 20 °C
6: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere
7: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C
With
dmap; copper(I) bromide dimethylsulfide complex; palladium 10% on activated carbon; tetrabutyl ammonium fluoride; hydrogen; oxygen; copper(II) sulfate; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; hydrazine; diethylazodicarboxylate;
In
tetrahydrofuran; perdeuteriopyridine; diethyl ether; ethanol; dichloromethane; ethyl acetate;
DOI:10.1021/jo4006602