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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635005Generated: October 29, 2026

Benzoyl chloride → HCID 15887617, compound

https://huagongshe.com/reaction/635005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant6-(4-chloro-2-methylphenoxy)pyridin-3-amineHCID 2800143—
SolventDichloromethaneHCID 6344—
ProductHCID 15887617HCID 15887617—

Reaction Conditions

Temperature22 °C

Reaction Steps

2-(4-Chloro-2-methyl-phenoxy)-5-aminopyridine (211 mg, 0.90 mmol) was dissolved in methylene chloride (2.7 mL) then treated with triethylamine (0.19 mL, 1.35 mmol) followed by benzoyl chloride (0.13 mL, 1.12 mmol). The reaction mixture was stirred for 3 hours at 22° C. then saturated aqueous NaHCO3 was added and the mixture was stirred for another hour. The organic layer was separated and washed 2× with 6% aqueous NaHCO3, dried over Na2SO4 and concentrated in vacuo. The residue was chromatographed on silica gel using 1:1 ethyl acetate/hexane as eluent. The product was recovered as a white solid. MS (m/z): 338/340 (M+H)+; C19H15N2O2Cl requires 338.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184237B2
Source datasetuspto-grants-2001_02
ORD IDord-5e147d33434e4be88338528c8cd34878
Source noteuspto-grants-2001_02