(4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetic acid

Base Information

Chemical Name:(4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetic acid
CAS No.:1375701-93-1
Molecular Formula:C₂₄H₂₁ClFN₅O₂
Molecular Weight:465.914
Hs Code.:

Synonyms:(4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetic acid

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Chemical Property of (4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetic acid

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Technology Process of (4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetic acid

There total 5 articles about (4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)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:

: 1375702-59-2
ethyl (4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetate

: 1375701-93-1
(4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetic acid

Guidance literature:: ethyl (4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetate; With water; sodium hydroxide; In ethanol; at 60 ℃; for 2h;

With hydrogenchloride; In water;

Reference yield:

: 14062-25-0
Ethyl 4-bromophenylacetate

: 1375701-93-1
(4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate / palladium diacetate; XPhos / ISOPROPYLAMIDE / 1 h / 150 °C / Inert atmosphere; Microwave irradiation

2: hydrogen / palladium hydroxide, 20 wt% on carbon / ethanol / 16 h / 760.05 Torr

3: N-ethyl-N,N-diisopropylamine / ISOPROPYLAMIDE / 1.5 h / 150 °C

4: sodium hydroxide; water / ethanol / 2 h / 60 °C

With water; hydrogen; caesium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; palladium hydroxide, 20 wt% on carbon; palladium diacetate; XPhos; In ethanol; ISOPROPYLAMIDE;

Reference yield:

: 1375702-42-3
ethyl [4-(4-benzylpiperazin-1-yl)phenyl]acetate

: 1375701-93-1
(4-{4-[5-(5-chloro-1H-benzimidazol-2-yl)-3-fluoropyridin-2-yl]piperazin-1-yl}phenyl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen / palladium hydroxide, 20 wt% on carbon / ethanol / 16 h / 760.05 Torr

2: N-ethyl-N,N-diisopropylamine / ISOPROPYLAMIDE / 1.5 h / 150 °C

3: sodium hydroxide; water / ethanol / 2 h / 60 °C

With water; hydrogen; N-ethyl-N,N-diisopropylamine; sodium hydroxide; palladium hydroxide, 20 wt% on carbon; In ethanol; ISOPROPYLAMIDE;