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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178418884 | HCID 178418884 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[(1,2-Dimethyl-1H-imidazol-4-yl)ethynyl]-2-methylpyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091222B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-05d081150e494ba1a9034aa8e3bd60ad |
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| Source note | uspto-grants-2006_08 |
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