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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750885Generated: October 26, 2026

Methyl iodide → 1H-Indazole, 1-methyl-6-nitro-

https://huagongshe.com/reaction/1750885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant6-NitroindazoleHCID 24239—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product1H-Indazole, 1-methyl-6-nitro-HCID 8129041%

Reaction Steps

NaH (1.47 g, 0.037 mol) was added to THF (25 mL) at 0° C. Separately, 6-nitro-1H-indazole (5.0 g, 0.031 mol) was dissolved in THF (25 mL) and the solution was slowly added to the solution prepared. Iodomethane (2.48 mL, 0.040 mol) was slowly added to the mixed solution at the same temperature, followed by stirring for 2 hours. The reaction solution was concentrated under reduced pressure, and added with water and ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The concentrated compound (1-methyl added (Rf=0.8):2-methyl added (Rf=0.3)=1:1) was purified using silica gel chromatography (ethyl acetate:hexane=1:1 (v/v)) to obtain the title compound (Rf=0.8, 2.22 g, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156852B2
Source datasetuspto-grants-2015_10
ORD IDord-805f158b89714ede9b8d9e65766c90a9
Source noteuspto-grants-2015_10