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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911780Generated: October 31, 2026

Hydrogen Peroxide → 6-(4-Methylthiazol-2-ylamino)-5-phenoxypyridin-3-ol

https://huagongshe.com/reaction/911780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantTriisopropyl borateHCID 21531—
Reactant5-Bromo-N-(4-methylthiazol-2-yl)-3-phenoxypyridin-2-amineHCID 24765543—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418348HCID 178418348—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product6-(4-Methylthiazol-2-ylamino)-5-phenoxypyridin-3-olHCID 24764518—

Reaction Conditions

Temperature-78 °C

Reaction Steps

N-(5-Bromo-3-phenoxypyridin-2-yl)-4-methylthiazol-2-amine (2.66 mmol) is dissolved in THF (30 mL) and cooled to −78° C. MeLi (2.07 mL, 3.32 mmol) is slowly added and the reaction mixture is stirred for 10 minutes. n-Butyllithium (1.33 mL, 3.32 mmol) is added and the reaction mixture is stirred for 15 minutes. Triisopropylborate (0.613 mL, 2.66 mmol) is added and the reaction mixture is stirred for 30 minutes. The reaction mixture is warmed to 0° C., and methanol (5 mL), 10% aqueous NaOH (5.1 mL, 12.8 mmol), and 30% aqueous H2O2 (1.27 mL, 13.3 mmol) are added. The reaction mixture is stirred at 0° C. for 1 hour, then purified by silica gel chromatography (10-20% EtOAc in hexanes) to afford 6-(4-methylthiazol-2-ylamino)-5-phenoxypyridin-3-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022223B2
Source datasetuspto-grants-2011_09
ORD IDord-d856fadf935d4c78a75a13a0d7fe9530
Source noteuspto-grants-2011_09