Technology Process of 1-(2,4-dihydroxy-5-isopropyl-phenyl)-5-(4-piperidin-1-ylmethyl-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid ethylamide
There total 16 articles about 1-(2,4-dihydroxy-5-isopropyl-phenyl)-5-(4-piperidin-1-ylmethyl-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid ethylamide which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
10 wt% Pd(OH)2 on carbon; hydrogen;
In
ethanol;
at 20 ℃;
for 4h;
under 760.051 Torr;
Sealed tube;
DOI:10.1021/jm401536b
- Guidance literature:
-
Multi-step reaction with 7 steps
1: tert.-butylnitrite; trimethylsilylazide / acetonitrile / 13 h / 0 - 20 °C
2: chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer / N,N-dimethyl-formamide / 12 h / 20 °C
3: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C
4: triethylamine / dichloromethane / 12.5 h / 0 - 20 °C
5: triethylamine / N,N-dimethyl-formamide / 20 °C
6: methanol / 48 h / 80 °C / Sealed tube
7: hydrogen; 10 wt% Pd(OH)2 on carbon / ethanol / 4 h / 20 °C / 760.05 Torr / Sealed tube
With
tert.-butylnitrite; chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer; trimethylsilylazide; 10 wt% Pd(OH)2 on carbon; tetrabutyl ammonium fluoride; hydrogen; triethylamine;
In
tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
2: |Huisgen Cycloaddition;
DOI:10.1021/jm401536b