関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydroxylamine | HCID 787 | — |
| 反応物 | Diethyl acetylenedicarboxylate | HCID 69803 | — |
| 反応物 | Benzyl 1-cyano-4-fluoro-4-(hydroxymethyl)cyclohexylcarbamate | HCID 67977046 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | HCID 178472246 | HCID 178472246 | 60.2% |
反応手順
A flask was charged with benzyl 1-cyano-4-fluoro-4-(hydroxymethyl)cyclohexylcarbamate, Intermediate 33, (13.0 g, 42.4 mmol), EtOH (100 mL) and aqueous hydroxylamine (26.0 mL, 424 mmol). The reaction was stirred at 80° C. under nitrogen for 2 hours. The mixture was concentrated and the resulting residue diluted with CH2Cl2, washed with brine, dried (MgSO4) and the solvent evaporated to provide a colorless oil. The oil was dissolved in EtOH (100 mL) to which diethyl acetylenedicarboxylate (13.54 mL, 85 mmol) was added. The reaction was stirred under nitrogen for one hour. The solution was concentrated and the residue was dissolved in CH2Cl2 then purified by silica gel column chromatography eluting with hexane/ethyl acetate (0 to 100%). The appropriate fractions were combined and evaporated to give the title compound (13.01 g, 25.5 mmol, 60.2% yield)] as a light yellow syrup.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08835411B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-84c4207b97494f619cee774f0d6465ba |
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| 出典メモ | uspto-grants-2014_09 |
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