(S)-2-{2-[1-(4-fluorophenyl)ethyl]-6-(pyrazin-2-ylamino)pyridin-4-yloxy}ethanol

Base Information

Chemical Name:(S)-2-{2-[1-(4-fluorophenyl)ethyl]-6-(pyrazin-2-ylamino)pyridin-4-yloxy}ethanol
CAS No.:1239358-99-6
Molecular Formula:C₁₉H₂₀FN₅O₂
Molecular Weight:369.399
Hs Code.:

Synonyms:(S)-2-{2-[1-(4-fluorophenyl)ethyl]-6-(pyrazin-2-ylamino)pyridin-4-yloxy}ethanol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-2-{2-[1-(4-fluorophenyl)ethyl]-6-(pyrazin-2-ylamino)pyridin-4-yloxy}ethanol

Chemical Property:

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Technology Process of (S)-2-{2-[1-(4-fluorophenyl)ethyl]-6-(pyrazin-2-ylamino)pyridin-4-yloxy}ethanol

There total 4 articles about (S)-2-{2-[1-(4-fluorophenyl)ethyl]-6-(pyrazin-2-ylamino)pyridin-4-yloxy}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:

: 1354807-11-6
(S)-4-chloro-N₂-[1-(4-fluorophenyl)ethyl]-N₆-(pyrazin-2-yl)pyridine-2,6-diamine

: 107-21-1
ethylene glycol

: 1239358-99-6
(S)-2-{2-[1-(4-fluorophenyl)ethyl]-6-(pyrazin-2-ylamino)pyridin-4-yloxy}ethanol

Guidance literature:: With potassium phosphate; XPhos; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; In water; at 100 ℃; for 13h; Inert atmosphere;

Reference yield:

: 16063-69-7
2,4,6-trichloropyridine

: 1239358-99-6
(S)-2-{2-[1-(4-fluorophenyl)ethyl]-6-(pyrazin-2-ylamino)pyridin-4-yloxy}ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / butan-1-ol / 42 h / 120 °C

2: potassium phosphate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex / 1,4-dioxane / 19 h / 100 °C / Inert atmosphere

3: potassium phosphate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 2 h / 100 °C

With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; potassium phosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; N-ethyl-N,N-diisopropylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; butan-1-ol;

Reference yield:

: 66399-30-2
(S)-1-(4-Fluoro-phenyl)-ethylamine

: 1239358-99-6
(S)-2-{2-[1-(4-fluorophenyl)ethyl]-6-(pyrazin-2-ylamino)pyridin-4-yloxy}ethanol

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / butan-1-ol / 42 h / 120 °C

2: potassium phosphate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex / 1,4-dioxane / 19 h / 100 °C / Inert atmosphere

3: potassium phosphate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 2 h / 100 °C

With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; potassium phosphate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; N-ethyl-N,N-diisopropylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; butan-1-ol;