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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579637Generated: October 31, 2026

Pyridine → 6-Methylpyridine-2-carboxylic acid (6-acetyl-3-methoxy-2-methylphenyl)-amide

https://huagongshe.com/reaction/579637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-Methylpyridine-2-carboxylic acidHCID 70282—
Reactant2'-Amino-3'-methyl-4'-methoxyacetophenoneHCID 25067316—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product6-Methylpyridine-2-carboxylic acid (6-acetyl-3-methoxy-2-methylphenyl)-amideHCID 5795639686.2%

Reaction Conditions

Temperature-5 °C

Reaction Steps

6-Methylpicolinic acid (1.12 g, 8.167 mmol) was dissolved in dry DCM (100 ml) and kept on an ice-bath. Then, 6-acetyl-3-methoxy-2-methylaniline (1.48 g, 8.17 mmol) and pyridine (6.6 mL, 0.082 mol) were added followed by drop wise addition of POCl3 (1.53 mL, 0.016 mol) over 15 minutes. The resulting solution was stirred at −5° C. for 1 h. Then, water (100 mL) was added carefully and after 5 min of stirring, NaOH (40%, 20 mL) was subsequently added drop wise followed by the separation of the organic layer. The water layer was extracted three times with CH2Cl2, and the combined organic layers were washed with brine, dried (MgSO4), filtered and evaporated. The residue was purified by column chromatography (Heptane/AcOEt, 3:1) to give the title compound (2.1 g, 86%): m/z=299 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040562B2
Source datasetuspto-grants-2015_05
ORD IDord-27c45eeb7fde4087ae06329ebf69dfb9
Source noteuspto-grants-2015_05