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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405082Generated: November 1, 2026

Methanol → 3,5-Dibromo-4-methoxypyridine

https://huagongshe.com/reaction/1405082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant3,4,5-TribromopyridineHCID 541462—
SolventWaterHCID 962—
Product3,5-Dibromo-4-methoxypyridineHCID 2176602695%

Reaction Steps

To a solution of MeOH (0.115 mL, 2.85 mmol) and THF (0.5 mL) at 0° C. was added sodium hydride (60% dispersion, 114 mg, 2.85 mmol). After stirring for 15 min, Intermediate 31B (600 mg, 1.900 mmol) was added, and the resulting mixture was stirred at room temperature for 19 hours, diluted with water (3 mL) and extracted with EtOAc (2×10 mL). The combined organics were washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to yield Intermediate 31 (0.480 g, 1.798 mmol, 95% yield) as a beige color solid. MS (ES): m/z=267.9 [M+H]+. 1H NMR (400 MHz, MeOD) δ ppm 8.68 (2 H, s), 3.99 (3 H, s). Intermediate 31 was used in the synthesis of Example 185.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916553B2
Source datasetuspto-grants-2014_12
ORD IDord-fd661e44a93042c69357db454fa04fd8
Source noteuspto-grants-2014_12