Technology Process of C33H46N4O3
There total 15 articles about C33H46N4O3 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 8 steps
1: palladium 10% on activated carbon; hydrogen / ethanol / 16 h / 20 °C / 760.05 Torr
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.25 h / 0 °C
3: CHIRAEPAKAD columnS cm I.Dx50 cm L / isopropyl alcohol; n-heptane / Resolution of racemate
4: pyridine / 2 h / 0 - 20 °C
5: triethylamine; copper(l) iodide; tri-tert-butyl phosphine; tetrakis(triphenylphosphine) palladium(0) / acetonitrile; hexane / 16 h / Inert atmosphere; Reflux
6: water; sodium hydroxide / tetrahydrofuran; methanol / 3 h / 20 °C
7: 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 16 h / 20 °C
8: palladium 10% on activated carbon; hydrogen; acetic acid / methanol / 12 h / 20 °C / 760.05 Torr
With
pyridine; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); tri-tert-butyl phosphine; palladium 10% on activated carbon; tetrabutyl ammonium fluoride; water; hydrogen; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; sodium hydroxide;
In
tetrahydrofuran; methanol; ethanol; hexane; n-heptane; isopropyl alcohol; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 7 steps
1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.25 h / 0 °C
2: CHIRAEPAKAD columnS cm I.Dx50 cm L / isopropyl alcohol; n-heptane / Resolution of racemate
3: pyridine / 2 h / 0 - 20 °C
4: triethylamine; copper(l) iodide; tri-tert-butyl phosphine; tetrakis(triphenylphosphine) palladium(0) / acetonitrile; hexane / 16 h / Inert atmosphere; Reflux
5: water; sodium hydroxide / tetrahydrofuran; methanol / 3 h / 20 °C
6: 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 16 h / 20 °C
7: palladium 10% on activated carbon; hydrogen; acetic acid / methanol / 12 h / 20 °C / 760.05 Torr
With
pyridine; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); tri-tert-butyl phosphine; palladium 10% on activated carbon; tetrabutyl ammonium fluoride; water; hydrogen; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; sodium hydroxide;
In
tetrahydrofuran; methanol; hexane; n-heptane; isopropyl alcohol; acetonitrile;
- Guidance literature:
-
Multi-step reaction with 6 steps
1: CHIRAEPAKAD columnS cm I.Dx50 cm L / isopropyl alcohol; n-heptane / Resolution of racemate
2: pyridine / 2 h / 0 - 20 °C
3: triethylamine; copper(l) iodide; tri-tert-butyl phosphine; tetrakis(triphenylphosphine) palladium(0) / acetonitrile; hexane / 16 h / Inert atmosphere; Reflux
4: water; sodium hydroxide / tetrahydrofuran; methanol / 3 h / 20 °C
5: 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 16 h / 20 °C
6: palladium 10% on activated carbon; hydrogen; acetic acid / methanol / 12 h / 20 °C / 760.05 Torr
With
pyridine; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); tri-tert-butyl phosphine; palladium 10% on activated carbon; water; hydrogen; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; 3-[(diethoxyphosphinyl)oxy]-1,2,3-benzotriazin-4(3H)-one; sodium hydroxide;
In
tetrahydrofuran; methanol; hexane; n-heptane; isopropyl alcohol; acetonitrile;