HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084288Generated: October 25, 2026
Methyl iodide → 4-Methoxy-1-(2-pyridyl)-3,6,6-trimethyl-4,5,6,7-tetrahydroindazole
https://huagongshe.com/reaction/2084288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Hydroxy-1-(2-pyridyl)-3,6,6-trimethyl-4,5,6,7-tetrahydroindazole | HCID 9816561 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methoxy-1-(2-pyridyl)-3,6,6-trimethyl-4,5,6,7-tetrahydroindazole | HCID 9860270 | 82% |
Reaction Steps
0.11 g (2.04 mmol) of 55% sodium hydride in oil were added to a solution of 4-hydroxy-1-(2-pyridyl)-3,6,6-trimethyl-4,5,6,7-tetrahydroindazole (0.35 g, 1.36 mmol), prepared as described in example 12, in dry tetrahydrofuran (5 ml) maintained under magnetic stirring and inhert atmosphere at 0° C. After 5 minutes, 0.13 ml (2.04 mmol) of methyl iodide were added, the reaction mixture was allowed to warm to room temperature and after 3.5 hours further 0.13 ml of methyl iodide were added. Stirring was continued for about 24 hours, additional sodium hydride (0.11 g) and methyl iodide (0.13 ml) were added and after 2.5 hours the solvent was evaporated. The residue was chromatographed on silica gel (cyclohexane:ethyl acetate=90:10), to yield the title compound as a colourless solid (0.3 g, 82%): m.p. 66-68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06716856B1 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-01568b4ca8ae4d27afe2f7af441656ff |
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| Source note | uspto-grants-2004_04 |
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