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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204313Generated: October 29, 2026

3-chloro-1-methyl-5-nitropyridin-2(1H)-one → 3-Amino-5-chloro-1-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/2204313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-chloro-1-methyl-5-nitropyridin-2(1H)-oneHCID 86703106—
Reactant5-Chloro-1-methyl-3-nitropyridin-2-oneHCID 86703119—
Product3-Amino-5-chloro-1-methylpyridin-2(1H)-oneHCID 86703118—

Reaction Steps

The title compound was prepared in analogy to the procedure for Step E5, but 5-chloro-1-methyl-3-nitro-1H-pyridin-2-one (Step L5) was used instead of 3-chloro-1-methyl-5-nitro-1H-pyridin-2-one to afford the title compound as a gray solid. ESI-MS: tR=0.54 min, [M+H]+ 159/161 (LC-MS 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-ab0fbb5ee20a458590582f8fc50e8f30
Source noteuspto-grants-2016_06