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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8862Generated: October 29, 2026

Water → 4-[(1,2-Dimethyl-1H-imidazol-4-yl)ethynyl]-2-methylpyridine

https://huagongshe.com/reaction/8862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178418884HCID 178418884—
SolventTetrahydrofuranHCID 8028—
Product4-[(1,2-Dimethyl-1H-imidazol-4-yl)ethynyl]-2-methylpyridineHCID 11148529—

Reaction Steps

Sodium hydride (76 mg, 55%, 1.57 mmol) was suspended in 2 mL of dry THF. A solution of 2-methyl-4-(2-methyl-1H-imidazol-4-ylethynyl)-pyridine (150 mg, 0.76 mmol) in 8 mL of dry THF was added and the reaction mixture was stirred at room temperature for 30 min. A solution of methyliodide (142 mg, 1.00 mmol) in 1 mL of dry THF was added and stirring was continued overnight. The reaction mixture was poured into 70 mL of water and extracted three times with ethyl acetate (70 mL each). The combined organic extracts were dried with sodium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (dichloromethane/methanol 100:0->90:10 gradient) and a mixture of two regioisomers was obtained. This mixture could be separated by HPLC (chiralpak AD, heptane/ethanol 4/1) and the desired compound was obtained as a white solid (40 mg, 25%), MS: m/e=212.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091222B2
Source datasetuspto-grants-2006_08
ORD IDord-05d081150e494ba1a9034aa8e3bd60ad
Source noteuspto-grants-2006_08