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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190625Generated: November 1, 2026

4-Bromo-3-chlorobenzoic acid → 3-Chloro-4-{4-[5-(1-ethyl-1H-indol-6-ylcarbamoyl)-pyridin-2-yl]-piperazin-1-yl}-benzoic acid

https://huagongshe.com/reaction/2190625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-3-chlorobenzoic acidHCID 12594302—
Reactant4-{4-[4-(3-tert-Butyl-phenylcarbamoyl)-2-fluoro-phenyl]-piperazin-1-yl}-benzoic acidHCID 59318193—
ReactantN-(1-ethyl-1H-indol-6-yl)-6-piperazin-1-yl-nicotinamideHCID 67355710—
Product3-Chloro-4-{4-[5-(1-ethyl-1H-indol-6-ylcarbamoyl)-pyridin-2-yl]-piperazin-1-yl}-benzoic acidHCID 46202644—

Reaction Steps

3-Chloro-4-{4-[5-(1-ethyl-1H-indol-6-ylcarbamoyl)-pyridin-2-yl]-piperazin-1-yl}-benzoic acid was synthesized from N-(1-ethyl-1H-indol-6-yl)-6-piperazin-1-yl-nicotinamide and 4-bromo-3-chloro-benzoic 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 C27H26ClN5O3 (m/e) 503, obsd 504 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324385B2
Source datasetuspto-grants-2012_12
ORD IDord-05001d0d1cd6402c86a1bba71cfcdeff
Source noteuspto-grants-2012_12