関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4H-pyran-4-one | HCID 7968 | — |
| 反応物 | Morpholine | HCID 8083 | — |
| 反応物 | 3-(4-Methylphenyl)-3-oxopropanenitrile | HCID 522513 | — |
| 反応物 | Sulfur | HCID 5362487 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-Methylbenzaldehyde | HCID 7725 | 76.9% |
反応手順
4-Pyranone (2.31 mL, 24.97 mmol) and sulphur (801 mg, 24.97 mmol) were added to a solution of 3-oxo-3-p-tolyl-propionitrile (3.79 g, 23.8 mmol) in ethanol (40 mL) followed by morpholine (2.18 mL, 24.97 mmol) and the reaction heated at 40° C. for 16 hours, The reaction mixture was concentrated in vacuo and the residue purified by flash chromatography on silica eluting with 0-20% ethylacetate/heptanes to afford 12-Amino-4,7-dihydro-5H-thieno[2,3-c]pyran-3-yl)-p-tolyl-methanone as a yellow solid (2.2 g, 36% yield). LCMS (2 min acidic) 1.07 min ES+/AP+ 274 (MH+). 1HNMR (400 MHz, CDCl3) δ ppm 2.00-2.03 (m, 2H), 2.42 (s, 3H), 3.80-3.84 (m, 2H), 4.80 (s, 2H), 6.60 (br s, 2H), 7.20 (d, 2H), 7.41 (d, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08809363B2 |
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| 出典データセット | uspto-grants-2014_08 |
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| ORD ID | ord-137b9c2d900f476f9a9343f506ac1196 |
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| 出典メモ | uspto-grants-2014_08 |
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