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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220178Generated: October 26, 2026

4-Bromoaniline → 2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid (4-bromo-phenyl)-amide

https://huagongshe.com/reaction/220178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanilineHCID 7807—
ReactantTriethylamineHCID 8471—
ReactantPyBroPHCID 2733179—
Reactant2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acidHCID 59238266—
SolventDichloromethaneHCID 6344—
Product2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid (4-bromo-phenyl)-amideHCID 59238294—

Reaction Steps

To a solution of 2-(5-Bromo-pyridin-2-yl)-5-chloro-pentanoic acid (1.9 g, 6.5 mmol), Et3N (3.6 mL, 26 mmol), and Pybrop (6 g, 13 mmol) in CH2Cl2 (30 mL) was added 4-bromo-phenylamine (1.45 g, 8.45 mmol). This mixture was stirred overnight at room temperature and then evaporated. The mixture was redissolved in EtOAc (40 mL) and washed with 2N HCl (20 mL×3), brine, 5% NaHCO3 (20 mL×3), brine, dried with Na2SO4, filtered and evaporated. The residue was purified by column chromatography on silica gel using hexane/EtOAc to give a white solid (1.63 g, 56% for two steps). MS: calc'd 444 (MH+), exp 444 (MH+). 1H NMR (400 MHz, CDCl3-d) 9.65 (broad s, 1H), 8.72 (d, 1H, J=2.0 Hz), 8.06 (d, 1H, J=8.4 Hz), 7.53-7.41 (m, 4H), 4.18-4.08 (m, 1H), 3.66-3.54 (m, 2H), 2.45-2.35 (m, 1H), 2.21-2.11 (m, 1H), 1.98-1.87 (m, 1H), 1.83-1.72 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202866B2
Source datasetuspto-grants-2012_06
ORD IDord-37abab0d833d4ed6b72a3cd9ac56a8c5
Source noteuspto-grants-2012_06