N-(3-((1H-benzo[d]imidazol-1-yl)methyl)-4-ethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-4-amine

Base Information

Chemical Name:N-(3-((1H-benzo[d]imidazol-1-yl)methyl)-4-ethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-4-amine
CAS No.:1569983-01-2
Molecular Formula:C₂₇H₂₅N₅O₂
Molecular Weight:451.528
Hs Code.:

Synonyms:N-(3-((1H-benzo[d]imidazol-1-yl)methyl)-4-ethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-4-amine

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Chemical Property of N-(3-((1H-benzo[d]imidazol-1-yl)methyl)-4-ethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-4-amine

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Technology Process of N-(3-((1H-benzo[d]imidazol-1-yl)methyl)-4-ethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-4-amine

There total 6 articles about N-(3-((1H-benzo[d]imidazol-1-yl)methyl)-4-ethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-4-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:

: 5720-06-9
2-Methoxyphenylboronic acid

: 1569983-01-2
N-(3-((1H-benzo[d]imidazol-1-yl)methyl)-4-ethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / water; 1,2-dimethoxyethane / 2 h / Inert atmosphere; Reflux

2: hydrogenchloride / tert-butyl alcohol; ethyl acetate / 5 h / Reflux

With hydrogenchloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate; In 1,2-dimethoxyethane; water; ethyl acetate; tert-butyl alcohol;

Reference yield:

: 1094892-37-1
3-(benzoimidazol-1-ylmethyl)-4-ethoxy-phenylamine

: 75634-03-6
4-chloro-6-(2-methoxy-phenyl)-pyrimidine

: 1569983-01-2
N-(3-((1H-benzo[d]imidazol-1-yl)methyl)-4-ethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-4-amine

Guidance literature:: With hydrogenchloride; In ethyl acetate; tert-butyl alcohol; for 5h; Reflux;

Reference yield:

: 455-88-9
5-nitro-2-fluorotoluene

: 1569983-01-2
N-(3-((1H-benzo[d]imidazol-1-yl)methyl)-4-ethoxyphenyl)-6-(2-methoxyphenyl)pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 5 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 48 h / Reflux

2: potassium carbonate / dichloromethane / Reflux

3: sodium / 3 h / Reflux

4: tin(II) chloride dihdyrate / ethanol / 3 h / Reflux

5: hydrogenchloride / tert-butyl alcohol; ethyl acetate / 5 h / Reflux

With hydrogenchloride; N-Bromosuccinimide; tin(II) chloride dihdyrate; 2,2'-azobis(isobutyronitrile); sodium; potassium carbonate; In tetrachloromethane; ethanol; dichloromethane; ethyl acetate; tert-butyl alcohol;