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3-Methoxybenzylamine → HCID 57754052、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Methoxybenzylamine | HCID 21156 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Trifluoromethanesulfonic acid, lithium salt | HCID 3664839 | — |
| 反応物 | (1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl ester | HCID 86616462 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | HCID 57754052 | HCID 57754052 | — |
反応手順
A solution of (1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl ester (0.03 g, 0.1 mmol) in acetonitrile (1 mL) was treated with lithium triflate (0.032 g, 0.2 mmol) and stirred at ambient temperature for 20 minutes. Then 3-methoxybenzylamine (0.016 mL, 0.12 mmol) was added to the reaction neat in one portion. The reaction was stirred at ambient temperature for 14 hours. The reaction was poured into saturated ammonium chloride solution (5 mL), extracted with ethyl acetate, the organic phase separated, dried (MgSO4) and the solvent removed at reduced pressure. The product was obtained as an oil and used without further purification (0.041 g, 94%). MS: 437 (M+H, 100%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07557137B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-102b0fd138274c048ebe5de232edecef |
| 出典メモ | uspto-grants-2009_07 |