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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738271Generated: October 30, 2026

Acetic Acid → 3-Amino-6-benzyloxy-2-methylaminopyridine

https://huagongshe.com/reaction/1738271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant6-Benzyloxy-2-methylamino-3-nitropyridineHCID 10491498—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
Product3-Amino-6-benzyloxy-2-methylaminopyridineHCID 10728118—

Reaction Steps

21.4 g of zinc were added to a solution of 8.50 of 6-benzyloxy-2-methylamino-3-nitropyridine (prepared as described in Preparation 92) in 360 ml of methanol, and then 8.5 ml of acetic acid were added dropwise. The resuluting mixture was then stirred at room temperature for one hour. At the end of this time, the reaction mixture was filtered to remove insoluble material. The filtrate was freed from the solvent by distillation under reduced pressure, and the resulting residue was dissolved in ethyl acetate. The solution was washed with an aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order. The organic layer was dried over anhydrous sodium sulfate and the solvent was removed by distillation under reduced pressure, to give 7.50 g of the title compound having Rf=0.63 (on silica gel thin layer chromatography using ethyl acetate as the developing solvent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962470
Source datasetuspto-grants-1999_10
ORD IDord-2e1e238ee2d642e194124d09008ab714
Source noteuspto-grants-1999_10