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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750887Generated: October 26, 2026

Methyl iodide → 1-Methyl-5-nitro-1H-indazole

https://huagongshe.com/reaction/1750887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant5-NitroindazoleHCID 21501—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-5-nitro-1H-indazoleHCID 28021142.2%

Reaction Steps

NaH (1.47 g, 36.8 mmol) was added to THF (40 mL) at 0° C. Separately, 5-nitroindazole (5.0 g, 30.6 mmol) was dissolved in THF (30 mL), and the mixed solution was slowly added to the prepared solution. Iodomethane (2.1 mL, 33.7 mmol) was added to the reaction solution at the same temperature, followed by stirring for 3 hours at room temperature. The reaction solution was concentrated under reduced pressure, and added with water and ethyl acetate. The reaction mixture was added with distilled water for quenching, diluted with ethyl acetate, and washed with distilled water. The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The concentrated compound (1-methyl added (Rf=0.3), 2-methyl added (Rf=0.1)) was purified using silica gel chromatography (ethyl acetate:hexane=1:1 (v/v)) to obtain the title compound (Rf=0.3, 2.29 g, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156852B2
Source datasetuspto-grants-2015_10
ORD IDord-d1f66e03f2c84699864a73b04b33168c
Source noteuspto-grants-2015_10