関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bupropion Hydrochloride | HCID 62884 | — |
| 反応物 | Morpholin-4-ol | HCID 165345 | — |
| 反応物 | 3'-Chloropropiophenone | HCID 587128 | — |
| 反応物 | 1,4-Dioxane dibromide | HCID 22225919 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | alpha-Bromo-3-chloropropiophenone | HCID 4992116 | 85% |
反応手順
The racemate of the morpholinol metabolite of bupropion hydrochloride ((+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride) may be synthesized by the following process. To 3′-chloropropiophenone (10.0 g, 0.06 mol) in dioxane (50 mL) was added a solution of dioxane dibromide (14.9 g, 0.06 mol) in dioxane (50 mL). The reaction mixture was stirred for 2 h at ambient temperature and poured into a mixture of ice and water (500 mL). The mixture was extracted several times with methylene chloride. The combined extracts were dried (Na2SO4) and concentrated in vacuo to give 14.8 g (85%) of 2-bromo-3′-chloropropiophenone as a pale yellow oil. This was used without further purification. NMR (300 Mhz, CDCl3); δ 7.99 (m, 1H), 7.90 (d, 1H), 7.57 (d, 1H), 7.44 (t, 1H), 5.22 (q, 1H), 1.91 (t, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07098206B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-27b58087e3844fdf8b955fa933d6ceab |
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| 出典メモ | uspto-grants-2006_08 |
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