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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190615Generated: November 2, 2026

2-(4-Bromophenyl)propanoic acid → (4-{4-[5-(3-tert-Butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazin-1-yl}-phenyl)-propionic acid

https://huagongshe.com/reaction/2190615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Bromophenyl)propanoic acidHCID 521441—
ReactantN-(3-tert-Butyl-phenyl)-6-piperazin-1-yl-nicotinamideHCID 59318114—
Reactant4-{4-[4-(3-tert-Butyl-phenylcarbamoyl)-2-fluoro-phenyl]-piperazin-1-yl}-benzoic acidHCID 59318193—
Product(4-{4-[5-(3-tert-Butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazin-1-yl}-phenyl)-propionic acidHCID 67356842—

Reaction Steps

(4-{4-[5-(3-tert-Butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazin-1-yl}-phenyl)-propionic acid was synthesized from N-(3-tert-butyl-phenyl)-6-piperazin-1-yl-nicotinamide and 4-bromo phenyl propionic acid in a manner similar to the one described in the synthesis of 4-{4-[4-(3-tert-butyl-phenylcarbamoyl)-2-fluoro-phenyl]-piperazin-1-yl}-benzoic acid above. LCMS calcd for C29H34N4O3 (m/e) 486, obsd 487 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-84ffe3d3f8d84134adec6d52fc3445e0
Source noteuspto-grants-2012_12