Technology Process of 2-bromo-6-(1-oxo-3,4,6,7,8,9-hexahydropyrido[3,4-b]imidazo[4,5-c]pyridine-2-yl)benzyl acetate
There total 8 articles about 2-bromo-6-(1-oxo-3,4,6,7,8,9-hexahydropyrido[3,4-b]imidazo[4,5-c]pyridine-2-yl)benzyl acetate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
acetic acid 2,6-dibromobenzyl ester; 3,4,6,7,8,9-hexahydropyrido[3,4-b]imidazo[4,5-c]pyridine-1-one;
With
caesium carbonate;
copper(l) iodide;
In
1-methyl-pyrrolidin-2-one;
at 120 ℃;
for 16h;
Inert atmosphere;
acetyl chloride;
With
triethylamine;
In
dichloromethane;
at 20 ℃;
for 2h;
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: N-Bromosuccinimide / 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 14 h / 80 °C / Inert atmosphere
2.1: N,N-dimethyl-formamide / 14 h / 20 °C / Inert atmosphere
3.1: caesium carbonate / copper(l) iodide / 1-methyl-pyrrolidin-2-one / 16 h / 120 °C / Inert atmosphere
3.2: 2 h / 20 °C
With
N-Bromosuccinimide; caesium carbonate;
copper(l) iodide; 2,2'-azobis(isobutyronitrile);
In
1-methyl-pyrrolidin-2-one; tetrachloromethane; N,N-dimethyl-formamide;
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: ethanol / 2 h / 70 °C / Inert atmosphere
2.1: triethyl phosphite / 24 h / 110 °C / Inert atmosphere
3.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 1.5 h / 0 - 20 °C
4.1: acetic anhydride / 1.5 h / 140 °C / Inert atmosphere
5.1: hydrogen; acetic acid / palladium 10% on activated carbon / 48 h / 85 °C / 18100.7 Torr
5.2: pH 9
6.1: caesium carbonate / copper(l) iodide / 1-methyl-pyrrolidin-2-one / 16 h / 120 °C / Inert atmosphere
6.2: 2 h / 20 °C
With
hydrogen; acetic anhydride; caesium carbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; triethyl phosphite;
copper(l) iodide; palladium 10% on activated carbon;
In
1-methyl-pyrrolidin-2-one; ethanol; dichloromethane;