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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526167Generated: October 29, 2026

2-(Dimethylamino)ethanol → 6-[2-(Dimethylamino)ethoxy]pyridin-3-amine

https://huagongshe.com/reaction/526167

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-5-nitropyridineHCID 78308—
Solvent1,4-DioxaneHCID 31275—
Product6-[2-(Dimethylamino)ethoxy]pyridin-3-amineHCID 2069140661%

Reaction Steps

To a solution of 2-chloro-5-nitropyridine (500 mg, 3.1 mmol) in dioxane (30 mL) at room temperature was added 2-(dimethylamino)ethanol (309 mg, 3.5 mmol) and 60 wt. % NaH (0.15 g, 3.7 mmol) and the reaction mixture was stirred at room temperature until the reaction was complete by LCMS analysis. The reaction mixture was poured onto ice-cold water and the product was extracted with dichloromethane. The organic layer was dried over sodium sulfate, filtered and the filtrate was concentrated. The residue was dissolved in tetrahydrofuran (30 mL), degassed with nitrogen, charged with catalytic 10 wt. % Pd/C (0.3 g) and the reaction mixture was placed under an atmosphere of hydrogen (40 Psi) until the reduction was complete by LCMS analysis. The reaction mixture was filtered over diatomaceous earth and the filtrate was concentrated to provide the desired product (340 mg, 61%) as a purple solid: ESI MS m/z 182 [C9H15N3O+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345709B2
Source datasetuspto-grants-2016_05
ORD IDord-4311156f05cc4bbbade964c53f35ea7d
Source noteuspto-grants-2016_05