N-(2-ethyl-4-((2-methyl-1H-imidazol-1-yl)methyl)phenyl)-N,1-dimethyl-1H-imidazo[4,5-c]pyridin-6-amine

Base Information

Chemical Name:N-(2-ethyl-4-((2-methyl-1H-imidazol-1-yl)methyl)phenyl)-N,1-dimethyl-1H-imidazo[4,5-c]pyridin-6-amine
CAS No.:1449664-76-9
Molecular Formula:C₂₁H₂₄N₆
Molecular Weight:360.462
Hs Code.:

Synonyms:N-(2-ethyl-4-((2-methyl-1H-imidazol-1-yl)methyl)phenyl)-N,1-dimethyl-1H-imidazo[4,5-c]pyridin-6-amine

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Chemical Property of N-(2-ethyl-4-((2-methyl-1H-imidazol-1-yl)methyl)phenyl)-N,1-dimethyl-1H-imidazo[4,5-c]pyridin-6-amine

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Technology Process of N-(2-ethyl-4-((2-methyl-1H-imidazol-1-yl)methyl)phenyl)-N,1-dimethyl-1H-imidazo[4,5-c]pyridin-6-amine

There total 9 articles about N-(2-ethyl-4-((2-methyl-1H-imidazol-1-yl)methyl)phenyl)-N,1-dimethyl-1H-imidazo[4,5-c]pyridin-6-amine 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:

: 607373-83-1
2-chloro-4-methoxy-5-nitro-pyridine

: 1449664-76-9
N-(2-ethyl-4-((2-methyl-1H-imidazol-1-yl)methyl)phenyl)-N,1-dimethyl-1H-imidazo[4,5-c]pyridin-6-amine

Guidance literature:: Multi-step reaction with 7 steps

1.1: tetrahydrofuran / 2 h / 20 °C

2.1: iron; acetic acid / 1 h / 50 - 80 °C

3.1: 4 h / 100 °C

4.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; sodium t-butanolate / 1,4-dioxane / 4 h / 85 °C

5.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 °C / Inert atmosphere

5.2: 0 - 20 °C

6.1: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

7.1: N,N-dimethyl-formamide / 5 h / 100 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; lithium aluminium tetrahydride; iron; sodium hydride; acetic acid; sodium t-butanolate; XPhos; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1449664-56-5
(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)methanol

: 13551-83-2
bis-(2-methyl-1H-imidazol-1-yl)methanone

: 1449664-76-9
N-(2-ethyl-4-((2-methyl-1H-imidazol-1-yl)methyl)phenyl)-N,1-dimethyl-1H-imidazo[4,5-c]pyridin-6-amine

Guidance literature:: In N,N-dimethyl-formamide; at 100 ℃; for 5h;

Reference yield:

: 51688-75-6
4-amino-3-ethylbenzoic acid

: 1449664-76-9
N-(2-ethyl-4-((2-methyl-1H-imidazol-1-yl)methyl)phenyl)-N,1-dimethyl-1H-imidazo[4,5-c]pyridin-6-amine

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogenchloride / 1,4-dioxane / 16 h / 65 °C

2.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; sodium t-butanolate / 1,4-dioxane / 4 h / 85 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0 °C / Inert atmosphere

3.2: 0 - 20 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

5.1: N,N-dimethyl-formamide / 5 h / 100 °C

With hydrogenchloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; lithium aluminium tetrahydride; sodium hydride; sodium t-butanolate; XPhos; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide; mineral oil;