Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl iodide → 6-Bromo-1-methyl-1H-indazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 6-Bromo-1H-indazole | HCID 17842471 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 6-bromo-2-methyl-2H-indazole | HCID 22558624 | 43% |
| 생성물 | 6-Bromo-1-methyl-1H-indazole | HCID 22558675 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07772263B2 |
| 출처 데이터셋 | uspto-grants-2010_08 |
| ORD ID | ord-11ee07161b1848069adbb6445ffc0db4 |
| 출처 메모 | uspto-grants-2010_08 |