関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Carbonate Ion | HCID 19660 | — |
| 反応物 | Sodium Sulfate | HCID 24436 | — |
| 反応物 | Bismuth trichloride | HCID 24591 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | (2-(Trifluoromethyl)oxiran-2-yl)methyl 4-methylbenzenesulfonate | HCID 24809749 | — |
| 反応物 | 1-phenyl-1H-indazol-4-amine | HCID 24938057 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-Phenyl-N-{[2-(trifluoromethyl)-2-oxiranyl]methyl}-1H-indazol-4-amine | HCID 24938053 | 56.8% |
反応手順
Bismuth chloride (623 mg, 1.98 mmol) was added to a suspension of [2-(trifluoromethyl)-2-oxiranyl]methyl 4-methylbenzenesulfonate (5.85 g, 19.76 mmol) and 1-phenyl-1H-indazol-4-amine (4.13 g, 19.76 mmol) in dry dichloromethane (8 ml) and the mixture stirred at room temperature over the weekend. The resulting thick suspension was diluted with dichloromethane and stirred overnight. The mixture was then diluted with chloroform (200 ml) and sodium sulphate (30 g) and polymer supported carbonate resin (Fluka, ca. 3.5 mmoles carbonate/g resin, 11 g) were added and the mixture stirred overnight. LCMS showed no evidence for cyclisation to the target epoxide. Dry tetrahydrofuran (50 ml) and N,N-diisopropylethylamine (0.85 ml, 4.88 mmol) were then added and the mixture stirred overnight when LCMS indicated complete reaction. The mixture was filtered and the filtrate was washed with water. The aqueous phase was back-extracted with dichloromethane and the combined organic phases were dried and evaporated to give crude product which was purified by silica gel chromatography using the Flashmaster II (2×100 g cartridges) eluting with a 0 to 50% dichloromethane:ethyl acetate gradient over 40 minutes to give the title compound (3.74 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07947727B2 |
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| 出典データセット | uspto-grants-2011_05 |
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| ORD ID | ord-8ffb26c219254c14a3bd6cb2cf47a1ae |
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| 出典メモ | uspto-grants-2011_05 |
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