Technology Process of C49H60N8O6
There total 14 articles about C49H60N8O6 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at 0 - 20 ℃;
for 10h;
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: pyridine / dichloromethane / 2 h / 0 - 20 °C
2.1: tetrakis(triphenylphosphine) palladium(0); potassium carbonate / 1,2-dimethoxyethane; water / 5 h / 90 °C
3.1: t-butyldimethylsiyl triflate; N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C / Cooling with ice
3.2: 4 h / 0 °C
4.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 1 h / 20 °C / Cooling with ice
5.1: ammonium acetate / 5,5-dimethyl-1,3-cyclohexadiene / 5 h / 140 °C / Sealed tube
6.1: hydrogenchloride / ethyl acetate / 20 °C
7.1: N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine / dichloromethane / 10 h / 0 - 20 °C
With
pyridine; hydrogenchloride; tetrakis(triphenylphosphine) palladium(0); t-butyldimethylsiyl triflate; ammonium acetate; potassium carbonate; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine;
In
1,2-dimethoxyethane; 5,5-dimethyl-1,3-cyclohexadiene; dichloromethane; water; ethyl acetate; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 3 steps
1: ammonium acetate / 5,5-dimethyl-1,3-cyclohexadiene / 5 h / 140 °C / Sealed tube
2: hydrogenchloride / ethyl acetate / 20 °C
3: N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine / dichloromethane / 10 h / 0 - 20 °C
With
hydrogenchloride; ammonium acetate; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine;
In
5,5-dimethyl-1,3-cyclohexadiene; dichloromethane; ethyl acetate;