Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861497Generated: November 1, 2026

Pyridine → 4-bromo-N-cyclopropyl-2-methylbenzamide

https://huagongshe.com/reaction/1861497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantCyclopropylamineHCID 69828—
Reactant4-Bromo-2-methylbenzoic acidHCID 99570—
SolventEthyl AcetateHCID 8857—
Product4-bromo-N-cyclopropyl-2-methylbenzamideHCID 22568840—

Reaction Steps

A solution of 4-bromo-2-methylbenzoic acid and SOCl2 was refluxed for 3 hours, cooled to room temperature and concentrated under reduced pressure. The residue was dissolved in 30 mL CH2Cl2 and combined with cyclopropyl amine (810.0 mg, 14.3 mmols) and pyridine (2.05 g, 26.0 mmols). The solution was stirred for 18 hours and then diluted with EtOAc before being washed with 5% aqueous HCl, saturated NaHCO3, and saturated aqueous NaCl. The solution was dried (MgSO4) and concentrated under reduced pressure leaving the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531599B2
Source datasetuspto-grants-2003_03
ORD IDord-204d512fb9b34c9d9db85156862ae3e0
Source noteuspto-grants-2003_03