関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrogen Bromide | HCID 260 | — |
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | Methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrate | HCID 18918633 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | HCID 18918378 | HCID 18918378 | — |
反応手順
A mixture of methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrate (50 mg), 48% w/v hydrobromic acid (0.74 ml), dioxane (1 ml) and water (3 ml) was heated at 95° C. for 4 hours. The solution was cooled, diluted with water and freeze-dried to give the title compound, 40 mg, as a pale yellow solid: m.p. 163°-167° C.; NMR (D2O) δ8.40 (2H, d), 8.16 (2H, d), 7.40 (2H, d), 7.21 (2H, d), 5.21 (2H, s), 4 32 (4H, b), 3 89 (4H, bt), 1.86 (6H s); m/e 384 (M+H)+ ; calculated for C21H25N3.2HBr.2H2O: C, 43.3; H, 5.3; N, 7.2. found: C, 43.6; H, 5.3; N, 7.3%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05556977 |
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| 出典データセット | uspto-grants-1996_09 |
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| ORD ID | ord-3ad40ee7981f4be3b2915728deb31c22 |
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| 出典メモ | uspto-grants-1996_09 |
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