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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-Hydroxy-1-(2-pyridyl)-3,6,6-trimethyl-4,5,6,7-tetrahydroindazoleHCID 9816561—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-1-(2-pyridyl)-3,6,6-trimethyl-4,5,6,7-tetrahydroindazoleHCID 986027082%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716856B1
Source datasetuspto-grants-2004_04
ORD IDord-01568b4ca8ae4d27afe2f7af441656ff
Source noteuspto-grants-2004_04