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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626524Generated: October 31, 2026

Ammonium Chloride → 3-(4-((6-Amino-2-methylpyridin-3-yl)oxy)pyridin-2-yl)-1,1-dimethylurea

https://huagongshe.com/reaction/626524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1,1-Dimethyl-3-(4-((2-methyl-6-nitropyridin-3-yl)oxy)pyridin-2-yl)ureaHCID 90409867—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-(4-((6-Amino-2-methylpyridin-3-yl)oxy)pyridin-2-yl)-1,1-dimethylureaHCID 9040985596.3%

Reaction Steps

A mixture of 1,1-dimethyl-3-(4-((2-methyl-6-nitropyridin-3-yl)oxy)pyridin-2-yl)urea (5.2 g, 16.4 mmol) in MeOH (60 mL) and THF (60 mL) was treated with NH4Cl (26.3 g, 492 mmol) and stirred vigorously at RT. Zinc dust (10.72 g, 164 mmol) was added portion-wise and the mixture was stirred at RT for 2 h. Additional portions of NH4Cl (5 g, 93 mmol) and zinc dust (1 g, 15 mmol) were added and stirring was continued overnight. The mixture was diluted with EtOAc and filtered. The filtered solids were washed with EtOAc. The combined filtrates were further filtered (2×) and concentrated to dryness. THF (150 mL) and thiol-modified silica gel (1.4 mmol/g loading, 22 g, 31 mmol) were added and the mixture was stirred at RT overnight. The solids were removed by filtration and washed with THF. The combined filtrates were concentrated to dryness to give 3-(4-((6-amino-2-methylpyridin-3-yl)oxy)pyridin-2-yl)-1,1-dimethylurea (4.54 g, 96%) as a foam. MS (ESI) m/z: 288.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309224B2
Source datasetuspto-grants-2016_04
ORD IDord-4dfe171ddd974316b5707505a69b9fd1
Source noteuspto-grants-2016_04