2-(2-(1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl)-4-(4-fluoro-3-methylphenyl)-1H-imidazol-1-yl)ethanol

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Chemical Name:2-(2-(1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl)-4-(4-fluoro-3-methylphenyl)-1H-imidazol-1-yl)ethanol
CAS No.:1446104-05-7
Molecular Formula:C₂₁H₂₄BrFN₆O
Molecular Weight:475.364
Hs Code.:

Synonyms:2-(2-(1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl)-4-(4-fluoro-3-methylphenyl)-1H-imidazol-1-yl)ethanol

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Chemical Property of 2-(2-(1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl)-4-(4-fluoro-3-methylphenyl)-1H-imidazol-1-yl)ethanol

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Technology Process of 2-(2-(1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl)-4-(4-fluoro-3-methylphenyl)-1H-imidazol-1-yl)ethanol

There total 6 articles about 2-(2-(1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl)-4-(4-fluoro-3-methylphenyl)-1H-imidazol-1-yl)ethanol 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: 88.9%

: 663193-80-4
5-bromo-6-chloro-pyrimidin-4-ylamine

: 2-[4-(4-fluoro-3-methylphenyl)-2-piperidin-4-ylimidazol-1-yl]ethanol hydrochloride

: 1446104-05-7
2-(2-(1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl)-4-(4-fluoro-3-methylphenyl)-1H-imidazol-1-yl)ethanol

Guidance literature:: With caesium carbonate; In dimethyl sulfoxide; at 100 ℃;

Reference yield:

: 1226803-00-4
tert-butyl 4-(4-bromo-1-(2-hydroxyethyl)-1H-imidazol-2-yl)piperidine-1-carboxylate

: 1446104-05-7
2-(2-(1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl)-4-(4-fluoro-3-methylphenyl)-1H-imidazol-1-yl)ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: bis-tributylphosphine palladium⁽⁰⁾; caesium carbonate / 1,4-dioxane; water / 5 h / 70 °C / Sealed tube

2: hydrogenchloride / 1,4-dioxane; methanol / 3 h / 20 °C

3: caesium carbonate / dimethyl sulfoxide / 100 °C

With hydrogenchloride; bis-tributylphosphine palladium⁽⁰⁾; caesium carbonate; In 1,4-dioxane; methanol; water; dimethyl sulfoxide;

Reference yield:

: 158654-96-7
4-(1H-imidazol-2-yl)-piperidine-1-carboxylic acid tert-butyl ester

: 1446104-05-7
2-(2-(1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl)-4-(4-fluoro-3-methylphenyl)-1H-imidazol-1-yl)ethanol

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-Bromosuccinimide / tetrahydrofuran / 0.25 h / -46 °C

2.1: potassium hydroxide / dimethyl sulfoxide / 1.5 h

2.2: 4 h

2.3: 0.33 h / 20 °C

3.1: bis-tributylphosphine palladium⁽⁰⁾; caesium carbonate / 1,4-dioxane; water / 5 h / 70 °C / Sealed tube

4.1: hydrogenchloride / 1,4-dioxane; methanol / 3 h / 20 °C

5.1: caesium carbonate / dimethyl sulfoxide / 100 °C

With hydrogenchloride; N-Bromosuccinimide; bis-tributylphosphine palladium⁽⁰⁾; caesium carbonate; potassium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; water; dimethyl sulfoxide;