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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112563Generated: October 26, 2026

Methyl iodide → 6-Bromo-1-methyl-1H-indazole

https://huagongshe.com/reaction/2112563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-1H-indazoleHCID 17842471—
SolventTetrahydrofuranHCID 8028—
Product6-bromo-2-methyl-2H-indazoleHCID 2255862443%
Product6-Bromo-1-methyl-1H-indazoleHCID 2255867551%

Reaction Steps

To 6-bromoindazole (402A) (5.0 g, 25.4 mmol) in THF (50 mL) was added sodium hydride (95%, 672 mg, 26.6 mmol) with ice bath cooling. The mixture was stirred for 30 minutes. Methyl iodide (6.36 mL, 102 mmol) was added at room temperature. The reaction mixture was quenched with ammonium chloride solution and the layers were separated. The aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with brine, dried over sodium sulfate and concentrated. Purification by column chromatography (SiO2, ethyl acetate/hexane gradient) afforded 1-methyl-6-bromoindazole (402B) (2.71 g, 51%) as a yellow oil and 2-methyl-6-bromoindazole (402C) (2.28 g, 43%) as a yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524842B2
Source datasetuspto-grants-2009_04
ORD IDord-588c98c774694becb0aeae6eb415fe31
Source noteuspto-grants-2009_04