Technology Process of C23H38FN3O5S*ClH
There total 5 articles about C23H38FN3O5S*ClH which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydrogenchloride;
In
diethyl ether; dichloromethane;
at 20 ℃;
for 0.5h;
DOI:10.1021/jm301443r
- Guidance literature:
-
Multi-step reaction with 3 steps
1: dichloromethane / 0.25 h / 20 °C
2: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C
3: hydrogenchloride / dichloromethane; diethyl ether / 0.5 h / 20 °C
With
hydrogenchloride; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine;
In
diethyl ether; dichloromethane;
DOI:10.1021/jm301443r
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: hydrogen bromide; acetic acid / 0.5 h / 20 °C
1.2: Dowex-Cl / 0.08 h / 20 °C
2.1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C
3.1: dichloromethane / 0.25 h / 20 °C
4.1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C
5.1: hydrogenchloride / dichloromethane; diethyl ether / 0.5 h / 20 °C
With
hydrogenchloride; hydrogen bromide; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; acetic acid; N-ethyl-N,N-diisopropylamine;
In
diethyl ether; dichloromethane;
DOI:10.1021/jm301443r