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Trifluoromethanesulfonic anhydride → Trifluoro-methanesulfonic Acid Quinoxalin-5-yl Ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| 反応物 | 5-Quinoxalinol | HCID 135690274 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | Trifluoro-methanesulfonic Acid Quinoxalin-5-yl Ester | HCID 58611956 | 85.1% |
反応手順
Add trifluoromethanesulfonic anhydride (0.66 mL, 3.94 mmol) to a solution of quinoxalin-5-ol (Yamamoto, T. et al., J. Am. Chem. Soc. 1996, 118, 3930-3936; 500 mg, 3.42 mmol) in pyridine (6.8 mL) at 0° C. Allow the reaction to warm slowly to room temperature over 18 h. Add saturated aqueous sodium bicarbonate solution (100 mL) and extract the mixture with methylene chloride (3×100 mL). Dry the combined organic solutions with sodium sulfate, concentrate in vacuo, and purify by flash column chromatography to provide the subtitled compound (810 mg, 85%) as an off-white solid. MS ESI+ m/e 279 (M+1). 1H NMR (CDCl3): δ 8.85 (m, 2H), 8.18 (m, 1H), 7.84 (m, 1H), 7.63 (m, 1H). TLC (SiO2): Rf0.2 (3:1 hexanes/ethyl acetate).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07405299B2 |
| 出典データセット | uspto-grants-2008_07 |
| ORD ID | ord-563b5d0e08314816806c971745378742 |
| 出典メモ | uspto-grants-2008_07 |