2-amino-5-(4-methoxybenzyl)-4-[methoxy-(4-methoxyphenyl)]methyl-1-methyl-1H-imidazole

Base Information

Chemical Name:2-amino-5-(4-methoxybenzyl)-4-[methoxy-(4-methoxyphenyl)]methyl-1-methyl-1H-imidazole
CAS No.:1206617-54-0
Molecular Formula:C₂₁H₂₅N₃O₃
Molecular Weight:367.448
Hs Code.:

Synonyms:2-amino-5-(4-methoxybenzyl)-4-[methoxy-(4-methoxyphenyl)]methyl-1-methyl-1H-imidazole

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Chemical Property of 2-amino-5-(4-methoxybenzyl)-4-[methoxy-(4-methoxyphenyl)]methyl-1-methyl-1H-imidazole

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Technology Process of 2-amino-5-(4-methoxybenzyl)-4-[methoxy-(4-methoxyphenyl)]methyl-1-methyl-1H-imidazole

There total 5 articles about 2-amino-5-(4-methoxybenzyl)-4-[methoxy-(4-methoxyphenyl)]methyl-1-methyl-1H-imidazole 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: 98.0%

: 1206617-53-9
2-azido-5-[4-methoxybenzyl]-4-[methoxy-(4-methoxy-phenyl)]methyl-1-methyl-1H-imidazole

: 1206617-54-0
2-amino-5-(4-methoxybenzyl)-4-[methoxy-(4-methoxyphenyl)]methyl-1-methyl-1H-imidazole

Guidance literature:: With palladium on activated charcoal; hydrogen; In ethanol;
DOI:10.1016/j.tetlet.2009.10.117

Reference yield:

: 1197054-82-2
(4-iodo-1-methyl-1H-imidazol-5-yl)(4-methoxyphenyl)methanol

: 1206617-54-0
2-amino-5-(4-methoxybenzyl)-4-[methoxy-(4-methoxyphenyl)]methyl-1-methyl-1H-imidazole

Guidance literature:: Multi-step reaction with 6 steps

1.1: trifluoroacetic acid; triethylsilane / dichloromethane / 60 h / Inert atmosphere; Reflux

2.1: ethylmagnesium bromide / tetrahydrofuran / 2 h / 0 - 20 °C

2.2: 0 - 20 °C

3.1: magnesium / tetrahydrofuran

3.2: Reflux

4.1: trifluoroacetic acid / 55 °C

5.1: 4-toluenesulfonyl azide; n-butyllithium / hexane; tetrahydrofuran / -78 °C

6.1: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C / 760.05 Torr

With triethylsilane; n-butyllithium; 4-toluenesulfonyl azide; palladium 10% on activated carbon; ethylmagnesium bromide; hydrogen; magnesium; trifluoroacetic acid; In tetrahydrofuran; ethanol; hexane; dichloromethane;
DOI:10.1016/j.bmc.2017.01.024

Reference yield:

: 123-11-5
4-methoxy-benzaldehyde

: 1206617-54-0
2-amino-5-(4-methoxybenzyl)-4-[methoxy-(4-methoxyphenyl)]methyl-1-methyl-1H-imidazole

Guidance literature:: Multi-step reaction with 7 steps

1.1: ethylmagnesium bromide / dichloromethane

2.1: trifluoroacetic acid; triethylsilane / dichloromethane / 60 h / Inert atmosphere; Reflux

3.1: ethylmagnesium bromide / tetrahydrofuran / 2 h / 0 - 20 °C

3.2: 0 - 20 °C

4.1: magnesium / tetrahydrofuran

4.2: Reflux

5.1: trifluoroacetic acid / 55 °C

6.1: 4-toluenesulfonyl azide; n-butyllithium / hexane; tetrahydrofuran / -78 °C

7.1: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C / 760.05 Torr

With triethylsilane; n-butyllithium; 4-toluenesulfonyl azide; palladium 10% on activated carbon; ethylmagnesium bromide; hydrogen; magnesium; trifluoroacetic acid; In tetrahydrofuran; ethanol; hexane; dichloromethane;
DOI:10.1016/j.bmc.2017.01.024