[5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)-pyrimidin-2-yl]-(4-methoxy-phenyl)-amine

Base Information

Chemical Name:[5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)-pyrimidin-2-yl]-(4-methoxy-phenyl)-amine
CAS No.:1072930-29-0
Molecular Formula:C₂₁H₂₀FN₅O
Molecular Weight:377.421
Hs Code.:

Synonyms:[5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)-pyrimidin-2-yl]-(4-methoxy-phenyl)-amine

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Chemical Property of [5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)-pyrimidin-2-yl]-(4-methoxy-phenyl)-amine

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Technology Process of [5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)-pyrimidin-2-yl]-(4-methoxy-phenyl)-amine

There total 6 articles about [5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)-pyrimidin-2-yl]-(4-methoxy-phenyl)-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: 8.0%

: 1072928-93-8
5-fluoro-N₁-propylbenzene-1,2-diamine

: 946670-18-4
2-(4-methoxy-phenylamino)-pyrimidine-5-carboxylic acid

: 1072930-29-0
[5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)-pyrimidin-2-yl]-(4-methoxy-phenyl)-amine

Guidance literature:: 2-(4-methoxy-phenylamino)-pyrimidine-5-carboxylic acid; With thionyl chloride; at 80 ℃; for 0.25h;

5-fluoro-N₁-propylbenzene-1,2-diamine; In tetrahydrofuran; at 70 ℃; for 16h;

Reference yield:

: [5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)pyrimidin-2-yl](4-methoxyphenyl)amine hydrochloride

: 1072930-29-0
[5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)-pyrimidin-2-yl]-(4-methoxy-phenyl)-amine

Guidance literature:: With sodium hydroxide; In water;

Reference yield:

: 446-35-5
2,4-Difluoronitrobenzene

: 1072930-29-0
[5-(6-fluoro-1-propyl-1H-benzoimidazol-2-yl)-pyrimidin-2-yl]-(4-methoxy-phenyl)-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / tetrahydrofuran / 18 h / 20 °C

2.1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran / 96 h / 20 °C

3.1: thionyl chloride / 0.25 h / 80 °C

3.2: 16 h / 70 °C

With thionyl chloride; hydrogen; potassium carbonate; palladium 10% on activated carbon; In tetrahydrofuran;