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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200107Generated: November 1, 2026

Methyl iodide → 2-chloro-N-(3-fluoro-4-nitro-phenyl)-N-methyl-pyridin-4-amine

https://huagongshe.com/reaction/2200107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-N-(3-fluoro-4-nitrophenyl)-4-pyridinamineHCID 90020614—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-chloro-N-(3-fluoro-4-nitro-phenyl)-N-methyl-pyridin-4-amineHCID 9002047760.2%

Reaction Steps

Add 2-chloro-N-(3-fluoro-4-nitro-phenyl)pyridin-4-amine (300 mg, 1.12 mmol), methyl iodide (174 mg, 1.23 mmol) and K2CO3 (201 mg, 1.45 mmol) in DMF (6 mL). Stir the reaction at 70° C. for 3 hrs. TLC (EtOAc:PE=1:1) shows the reaction is complete, cool the reaction to 0° C., add water, extract with EtOAc. Combine the organic layers. Wash with brine, dry over anhydrous Na2SO4. Concentrate to give the crude product. Purification by chromatography (silica gel, EtOAc:PE=1:1) affords the title compound (190 mg, 45%). MS: (M+1): 282.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359338B2
Source datasetuspto-grants-2016_06
ORD IDord-55e8c8b8674f45baa7952608fe395ac5
Source noteuspto-grants-2016_06