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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685109Generated: November 1, 2026

Sodium hydride → HCID 59292302, compound

https://huagongshe.com/reaction/1685109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Methoxy-1-propanolHCID 74116—
Reactant2-Amino-6-chloropyridineHCID 206246—
SolventDimethylformamideHCID 6228—
ProductHCID 59292302HCID 59292302—

Reaction Conditions

Temperature90 °C

Reaction Steps

Into a 250 mL round bottom flask was added 3-methoxy-propanol (5.26 g, 58.4 mmol) and DMF (156 mL). Sodium hydride (60%, 4.67 g, 3 eq) was added slowly to the solution. After addition the mixture was heated to 90° C. for one hour. 2-chloro-6-amino-pyridine was added and the mixture was heated to reflux for four hours. LCMS showed conversion to product. The reaction was cooled to room temperature and solvent was removed under vacuum. The residue was partitioned between water and ethyl acetate. Organic layer was separated and the aqueous was extracted three times with ethyl acetate (3×50 mL). Organic layer dried over sodium sulfate and filtered; the solvent was removed under vacuum. The residue was dissolved with 2N HCl in MeOH and stirred for five hours at room temperature; the solvent was removed and the residue was purified by column chromatography with 20% ethyl acetate in hexanes yielding 3.12 g (45%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148367B2
Source datasetuspto-grants-2012_04
ORD IDord-3069fec3f00f48b7b746b5429ec6f42e
Source noteuspto-grants-2012_04