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N-bromobutanimide → (5-bromo-1-methyl-1H-imidazol-2-yl)methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | (1-methyl-1H-imidazol-2-yl)methanol | HCID 573612 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (5-bromo-1-methyl-1H-imidazol-2-yl)methanol | HCID 23445171 | 67% |
反応手順
1-Methylimidazole-2-methanol (3.15 g, 28 mmol) (R. J. Sundberg; P. V. Nguyen; Med. Chem. Res. 7, 2, 1997, 123-136) was suspensed in THF (75 ml) at −20° C. and treated slowly (within 30 min) with N-bromosuccinimide (4.9 g, 27 mmol). The reaction mixture was allowed to warm up slowly to room temperature and quenched with saturated aqueous NaHCO3 solution (50 ml). The aqueous layer was extracted 3 times with AcOEt. The combined extracts were washed with saturated aqueous NaHCO3 solution, dried over Na2SO4, filtered and the solvent was removed in vacuo. The residue was chromatographed (silica, elution first with AcOEt/hexane 1:1, then with CH2Cl2/MeOH 95:05) to provide the title compound (2.11 g, 67%) as a white solid. MS: m/e=191.2 (M+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06610723B2 |
| 出典データセット | uspto-grants-2003_08 |
| ORD ID | ord-8ad3e346f50746bc81bc84d5ea1bcb29 |
| 出典メモ | uspto-grants-2003_08 |