참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzonitrile | HCID 7505 | — |
| 반응물 | 3-Methyl-5-phenyl-isoxazole-4-carboxylic acid methylamide | HCID 66663194 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Methyl-3,6-diphenyl-5H-isoxazolo[4,3-c]pyridin-4-one | HCID 22015565 | 48.9% |
반응 단계
159 mg (0.73 mmol) of 3-methyl-5-phenyl-isoxazole-4-carboxylic acid methylamide is suspended in 4 ml of THF under argon. At −5° C. a solution of butyl lithium (1.0 ml, 1.6M in hexane, 1.6 mmol, 2.2 eq.) is slowly added. After 1 h at this temperature, the solution is warmed to 0° C. and 0.92 ml (0.88 mmol, 1.2 eq.) of benzonitrile is slowly added. Under warming to room temperature, the red solution is stirred for another 2 h, then quenched with 0.1 ml of water and concentrated. The residue is then taken up in 4 ml of a 4M solution of HCl in dioxane and the suspension stirred for 16 h at room temperature. Then, the solvent is removed and the residue dissolved in ethyl acetate and carefully neutralised with sat. NaHCO3-solution. The phases are separated and the organic phases washed with brine, dried over Na2SO4 and concentrated. Chromatographic purification (hexane/ethyl acetate 90:10) yields 108 mg (48%) of 5-methyl-3,6-diphenyl-5H-isoxazolo[4,3-c]pyridin-4-one as a white solid. Mass spectrum: m/z (M+H)+: 303.2
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07087756B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-0e553ab04cd04660a202ef9b4f2450c0 |
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| 출처 메모 | uspto-grants-2006_08 |
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