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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302238Generated: October 31, 2026

Dimethylformamide → 6-chloro-N-[5-(3-dimethylaminobenzamido)-2-methylphenyl]pyridine-3-carboxamide

https://huagongshe.com/reaction/2302238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloronicotinoyl ChlorideHCID 2782165—
ReactantHCID 22057981HCID 22057981—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product6-chloro-N-[5-(3-dimethylaminobenzamido)-2-methylphenyl]pyridine-3-carboxamideHCID 986618514.9%

Reaction Steps

6-Chloropyrid-3-ylcarbonyl chloride (0.37 g) was added to a mixture of N-(3-amino4-methylphenyl)-3-dimethylaminobenzamide (0.54 g), potassium carbonate (0.304 g), DMF (5 ml) and methylene chloride (20 ml) and the resultant mixture was stirred at ambient temperature for 16 hours. The mixture was poured into water and extracted with ethyl acetate. The organic extracts were washed with a saturated aqueous sodium chloride solution, dried over magnesium sulphate and evaporated. The residue was purified by column chromatography on silica using a 3:2:1 mixture of isohexane, ethyl acetate and methylene chloride as eluent. There was thus obtained the title compound as a solid (0.122 g); NMR Spectrum: (DMSOd6) 2.19 (s, 6H), 3.28 (s, 3H), 6.88 (m, 1H), 7.25 (m, 4H), 7.57 (m, 1H), 7.7 (d, 1H), 7.84 (d, 1H), 8.36 (m, 1H), 8.95 (d,1H), 10.11 (s, 1H), 10.16 (s, 1H); Mass Spectrum: M+H+ 409 and 411.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432949B1
Source datasetuspto-grants-2002_08
ORD IDord-48035327f0504d319f58fde8c1c65fa6
Source noteuspto-grants-2002_08