関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzyloxyamine hydrochloride | HCID 102312 | — |
| 反応物 | 5'-Bromo-2'-(methylthio)spiro[cyclohexane-1,3'-[3H]indole] | HCID 21986266 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | HCID 178419047 | HCID 178419047 | — |
反応手順
5′-Bromo-2′-(methylthio)spiro[cyclohexane-1,3′-[3H]indole] (9.0 g, 28.98 mmol) and O-benzylhydroxylamine hydrochloride (13.8 g, 86.9 mmol) were combined in methanol (150 mL) and heated to 45° C. for 6 hours. Methanol was evaporated in vacuo. Ethyl acetate was added to the residue and this mixture was washed with ammonium chloride solution. Ethyl acetate was dried over magnesium sulfate, ethyl acetate collected evaporated in vacuo and the residue was flash chromatographed on alumina 90 (9:1 Hexane/EtOAc) to the desired product (6.5 g, 60%). 1H NMR (DMSO-d6, 300 MHz) δ 1.38–1.70 (m, 8H), 1.92–2.06 (m, 2H), 5.06 (s, 2H), 6.71 (d, 1H, J=8.26 Hz), 7.22–7.43 (m, 7H), 9.62 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07091234B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-2a5db7c4f64e47bcb8b812a4d9f7db0b |
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| 出典メモ | uspto-grants-2006_08 |
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