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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601838Generated: November 1, 2026

Methylamine → 6-chloro-N-methyl-3-nitropyridin-2-amine

https://huagongshe.com/reaction/1601838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSodium CarbonateHCID 10340—
Reactant2,6-Dichloro-3-nitropyridineHCID 85239—
SolventEthanolHCID 702—
Product6-chloro-N-methyl-3-nitropyridin-2-amineHCID 10750094—

Reaction Steps

20.0 ml of a 30% ethanolic solution of methylamine were added dropwise to a mixture of 29.0 g of 2,6-dichloro-3-nitropyridine, 300 ml of ethanol and 36.6 g of sodium carbonate, whilst cooling with ice, and the resulting mixture was stirred at room temperature for 8 hours. At the end of this time, the reaction mixture was freed from ethanol by distillation. The residue was diluted with water, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was crystallized by trituration with ethanol, to give 22.3 g of the title compound, melting at 114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977365
Source datasetuspto-grants-1999_11
ORD IDord-b21bdc9665fe40319660876b07fe44b3
Source noteuspto-grants-1999_11