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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007204Generated: October 25, 2026

Methyl iodide → 6-Chloro-N-(4-ethoxy-2-nitrophenyl)-N-methyl-3-pyridinecarboxamide

https://huagongshe.com/reaction/1007204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant6-Chloro-N-(4-ethoxy-2-nitrophenyl)-3-pyridinecarboxamideHCID 9840127—
ReactantSodium MethoxideHCID 10942334—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-Chloro-N-(4-ethoxy-2-nitrophenyl)-N-methyl-3-pyridinecarboxamideHCID 9902284—

Reaction Steps

To a solution of 6-chloro-N-(4-ethoxy-2-nitrophenyl)-3-pyridinecarboxamide (50 mg, 0.155 mmol) in DMF (2 ml) was added sodium methoxide (12 mg, 0.222 mmol) in DMF (1 ml) and the reaction mixture was stirred for 10 min. To the mixture was added iodomethane (22 mg, 0.155 mmol) slowly and the mixture was stirred for at room temperature for 3 h. It was diluted with ethyl acetate and washed with water and brine, dried over anhydrous sodium sulfate, and evaporated. The residue was purified by column chromatography to yield the titled compound as a light brown liquid. 1H NMR (CDCl3): 8.17 (d, J=2.1, 1H), 7.68-7.65 (m, 1H), 7.35 (d, J=2.7, 1H), 7.21 (t, J=7.8, 2H), 7.10-7.06 (m, 1H), 4.08-4.01 (m, 2H), 3.40 (s, 3H), 1.44 (t, J=6.9, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794397B2
Source datasetuspto-grants-2004_09
ORD IDord-2e9b5a0cb09742b5b398e9734a4ad3dd
Source noteuspto-grants-2004_09