Technology Process of C23H23N3O7
There total 5 articles about C23H23N3O7 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: thionyl chloride / dichloromethane / 0.5 h / 0 - 20 °C
1.2: 20 °C
2.1: triethylamine / dichloromethane / 20 °C
3.1: trifluoroacetic acid / dichloromethane / 2 h / 0 °C
4.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 0.5 h / Inert atmosphere
4.2: Inert atmosphere
With
thionyl chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid;
In
dichloromethane;
DOI:10.1002/cmdc.201100372
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: trifluoroacetic acid / dichloromethane / 2 h / 0 °C
2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 0.5 h / Inert atmosphere
2.2: Inert atmosphere
With
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid;
In
dichloromethane;
DOI:10.1002/cmdc.201100372
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: N,O-bis(trimethylsilyl)hydroxylamine; zinc trifluoromethanesulfonate / dichloromethane
2.1: thionyl chloride / dichloromethane / 0.5 h / 0 - 20 °C
2.2: 20 °C
3.1: triethylamine / dichloromethane / 20 °C
4.1: trifluoroacetic acid / dichloromethane / 2 h / 0 °C
5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 0.5 h / Inert atmosphere
5.2: Inert atmosphere
With
thionyl chloride; N,O-bis(trimethylsilyl)hydroxylamine; zinc trifluoromethanesulfonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid;
In
dichloromethane;
DOI:10.1002/cmdc.201100372