(1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid

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Chemical Name:(1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid
CAS No.:1388143-65-4
Molecular Formula:C₂₅H₂₁F₄N₅O₂
Molecular Weight:499.468
Hs Code.:

Synonyms:(1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid

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Chemical Property of (1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid

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Technology Process of (1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid

There total 3 articles about (1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid 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:

: 59184-90-6
ethyl (piperidin-4-yl)acetate

: 1388143-65-4
(1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate / N,N-dimethyl-formamide / 20 - 55 °C / Inert atmosphere

2: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; ethanol / 1 h / 150 °C / Inert atmosphere; Sealed; Microwave irradiation

3: water; lithium hydroxide / tetrahydrofuran; methanol / 20 °C / Sealed

With water; sodium carbonate; caesium carbonate; lithium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; ethanol; N,N-dimethyl-formamide;

Reference yield:

: 1388144-56-6
(1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid ethyl ester

: 1388143-65-4
(1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid

Guidance literature:: (1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid ethyl ester; With water; lithium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; Sealed;

With hydrogenchloride; In tetrahydrofuran; methanol; water;

Reference yield:

: 1370534-54-5
2-(6-bromopyridin-3-yl)-6-(trifluoromethyl)-1H-benzimidazole

: 1388143-65-4
(1-{5-[3-fluoro-4-(5-trifluoromethyl-1H-benzoimidazol-2-yl)phenyl]pyrazin-2-yl}piperidin-4-yl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / dimethyl sulfoxide / 18 h / 100 °C

2: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; ethanol / 1 h / 150 °C / Inert atmosphere; Sealed; Microwave irradiation

3: water; lithium hydroxide / tetrahydrofuran; methanol / 20 °C / Sealed

With water; potassium acetate; sodium carbonate; lithium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; ethanol; dimethyl sulfoxide;