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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385519Generated: October 31, 2026

Sodium Chloride → 3-Amino-6-chloro-2-(1,3-dioxolan-2-ylmethyl)aminopyridine

https://huagongshe.com/reaction/385519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant6-chloro-N-(1,3-dioxolan-2-ylmethyl)-3-nitropyridin-2-amineHCID 57815371—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product3-Amino-6-chloro-2-(1,3-dioxolan-2-ylmethyl)aminopyridineHCID 5781536773.5%

Reaction Steps

To a suspension of 13 g of iron powder in 650 mL of ethanol and 350 mL of water, 14 g of sodium chloride was added, and the mixture was heated under reflux while stirring for 20 minutes. Thereto was added 10 g of 6-chloro-N-(1,3-dioxolan-2-ylmethyl)-3-nitropyridin-2-amine at 65° C., and the mixture was heated under reflux while stirring for 30 minutes. The insoluble substance was filtered off, the solvent was distilled off to be 300 mL under reduced pressure, ethyl acetate was added thereto, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The resultant residue was purified by basic silica gel column chromatography using an eluent of ethyl acetate to obtain 6.5 g of 3-amino-6-chloro-2-(1,3-dioxolan-2-ylmethyl)aminopyridine as a light purple solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-e8598609ae344eabbc2888b2609bc8cf
Source noteuspto-grants-2013_02