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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331886Generated: October 25, 2026

2-Aminopyridine → HCID 68443709, compound

https://huagongshe.com/reaction/331886

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantIsoxazole, 4-(chloromethyl)-5-methyl-3-phenyl-HCID 11052826—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 68443709HCID 6844370918%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-aminopyridine (109 mg, 1.2 mmol) in THF (2 mL) was added potassium bis(trimethylsilyl)amide (0.9 M in THF, 1.2 mL, 1.1 mmol) at 0° C. under argon. After 10 min, a solution of 4-chloromethyl-5-methyl-3-phenyl-isoxazole (200 mg, 1.0 mmol) in THF (1 mL) was added and the resulting mixture stirred at 0° C. for 1 h. The mixture was then diluted with ethyl acetate (10 mL) and washed with water (10 mL) and brine (10 mL). The aqueous phase was extracted with ethyl acetate and the combined extracts dried over sodium sulfate, filtered and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate=4:1: to 1:1) afforded the title compound (45 mg, 18%) as an off white solid. MS: m/e=266.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877782B2
Source datasetuspto-grants-2014_11
ORD IDord-ebbe37abb20241489a6dd43910cb9ad7
Source noteuspto-grants-2014_11