3-(4-methoxybenzyl)-5-methyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine

Base Information

Chemical Name:3-(4-methoxybenzyl)-5-methyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine
CAS No.:1068659-93-7
Molecular Formula:C₁₆H₁₄F₃N₃O
Molecular Weight:321.302
Hs Code.:

Synonyms:3-(4-methoxybenzyl)-5-methyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine

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Chemical Property of 3-(4-methoxybenzyl)-5-methyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine

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Technology Process of 3-(4-methoxybenzyl)-5-methyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine

There total 3 articles about 3-(4-methoxybenzyl)-5-methyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine 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:

Reference yield: 77.0%

: 367-57-7
1,1,1-Trifluoro-2,4-pentanedione

: 88945-41-9
N-(Cyanmethyl)formimidsaeure-methylester

: 2393-23-9
4-methoxy-benzylamine

: 1068659-93-7
3-(4-methoxybenzyl)-5-methyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine

Guidance literature:: N-(Cyanmethyl)formimidsaeure-methylester; 4-methoxy-benzylamine; In dichloromethane; for 1.33333h; Inert atmosphere; Reflux;

1,1,1-Trifluoro-2,4-pentanedione; In dichloromethane; at 20 ℃; Reflux;
DOI:10.1021/jo102579g

Reference yield: 65.0%

: 367-57-7
1,1,1-Trifluoro-2,4-pentanedione

: 3-(4-methoxybenzyl)-3H-imidazol-4-ylamine

: 1068659-93-7
3-(4-methoxybenzyl)-5-methyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine

Guidance literature:: In dichloromethane; for 5h; Inert atmosphere; Schlenk technique; Reflux;
DOI:10.1055/s-0032-1317329

Reference yield:

: 2393-23-9
4-methoxy-benzylamine

: 1068659-93-7
3-(4-methoxybenzyl)-5-methyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 2 h / Inert atmosphere; Schlenk technique; Reflux

2: dichloromethane / 5 h / Inert atmosphere; Schlenk technique; Reflux

In dichloromethane;
DOI:10.1055/s-0032-1317329