Technology Process of C29H31N3O5
There total 3 articles about C29H31N3O5 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
2-amino-1-(3,4-dihydroquinolin-1(2H)-yl)ethanone;
With
O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine;
In
dichloromethane;
at 0 ℃;
for 0.25h;
Inert atmosphere;
(2S)-2-[(benzyloxycarbonyl)amino]-3-(4-methoxyphenyl)propanoic acid;
In
dichloromethane;
at 0 ℃;
for 0.166667h;
Inert atmosphere;
DOI:10.1039/c0ob00628a
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: palladium 10% on activated carbon; hydrogen / methanol / Inert atmosphere
2.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h / 0 °C / Inert atmosphere
2.2: 0.17 h / 0 °C / Inert atmosphere
With
palladium 10% on activated carbon; hydrogen; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine;
In
methanol; dichloromethane;
DOI:10.1039/c0ob00628a
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: 4-methyl-morpholine; chloroformic acid ethyl ester / tetrahydrofuran / 0.17 h / -20 °C / Inert atmosphere
1.2: 0.25 h / -20 °C / Inert atmosphere
2.1: palladium 10% on activated carbon; hydrogen / methanol / Inert atmosphere
3.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h / 0 °C / Inert atmosphere
3.2: 0.17 h / 0 °C / Inert atmosphere
With
4-methyl-morpholine; palladium 10% on activated carbon; hydrogen; chloroformic acid ethyl ester; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine;
In
tetrahydrofuran; methanol; dichloromethane;
DOI:10.1039/c0ob00628a