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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2112563생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2112563

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물6-Bromo-1H-indazoleHCID 17842471—
용매TetrahydrofuranHCID 8028—
생성물6-bromo-2-methyl-2H-indazoleHCID 2255862443%
생성물6-Bromo-1-methyl-1H-indazoleHCID 2255867551%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07524842B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-588c98c774694becb0aeae6eb415fe31
출처 메모uspto-grants-2009_04