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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521146Generated: October 27, 2026

2-Aminopyridine → (5-Methyl-3-phenyl-isoxazol-4-ylmethyl)-pyridin-2-yl-amine

https://huagongshe.com/reaction/1521146

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—
Product(5-Methyl-3-phenyl-isoxazol-4-ylmethyl)-pyridin-2-yl-amineHCID 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 numberUS09073908B2
Source datasetuspto-grants-2015_07
ORD IDord-deb03c25bc5e415bada43ce682da0f5a
Source noteuspto-grants-2015_07