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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Dimethylamino)ethanol | HCID 7902 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-[2-(Dimethylamino)ethoxy]pyridin-3-amine | HCID 20691406 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345709B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-4311156f05cc4bbbade964c53f35ea7d |
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| Source note | uspto-grants-2016_05 |
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