Technology Process of C23H26N4O2
There total 7 articles about C23H26N4O2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
C28H34N4O4;
With
trifluoroacetic acid;
In
dichloromethane;
at 20 ℃;
for 1.5h;
With
ammonia;
In
methanol; dichloromethane;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: ethylmagnesium bromide / diethyl ether; dichloromethane / 1 h / -20 °C
1.2: 0.5 h / -20 - 20 °C
2.1: methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 - 20 °C
2.2: 1.5 h / 65 °C
2.3: 20 °C
3.1: hydrogen / 10 % Pd(OH)2/C / methanol / 12 h / 2068.65 Torr
4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 20 °C
5.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C
With
ethylmagnesium bromide; hydrogen; methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid;
10 % Pd(OH)2/C;
In
methanol; diethyl ether; dichloromethane;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: formic acid / 2 h / 90 °C
2.1: ethylmagnesium bromide / diethyl ether; dichloromethane / 1 h / -20 °C
2.2: 0.5 h / -20 - 20 °C
3.1: methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 - 20 °C
3.2: 1.5 h / 65 °C
3.3: 20 °C
4.1: hydrogen / 10 % Pd(OH)2/C / methanol / 12 h / 2068.65 Torr
5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 20 °C
6.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C
With
formic acid; ethylmagnesium bromide; hydrogen; methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid;
10 % Pd(OH)2/C;
In
methanol; diethyl ether; dichloromethane;