関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 3,4-Dimethoxybenzenesulfonyl chloride | HCID 2734183 | — |
| 反応物 | 1(2H)-Isoquinolinone, 3-phenyl- | HCID 2752870 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | HCID 44322618 | HCID 44322618 | 46.7% |
反応手順
A solution of 3-phenylisocarbostyril (0.1 g) in N,N-dimethylformamide (2 ml) was cooled to 0° C. under an inert atmosphere. Sodium hydride (0.019 g) was added and the resulting mixture stirred at 0° C. for 5 minutes. 3,4-Dimethoxybenzenesulphonylchloride (0.107 g) was added over a 3 minute period, with continued stirring at 0° C. for a further 15 minutes. The reaction mixture was warmed to room temperature and stirred for 24 hours. The DMF was evaporated under high vacuum and the residue partitioned between ethyl acetate (2×12 ml) and water (12 ml). The combined organic phases were dried over magnesium sulphate and concentrated in vacuo to yield a yellow oil. Purification using column chromatography eluting with 50% ethyl acetate in hexane yielded an oil which was crystallized from ethyl acetate/hexane to furnish the title compound as white crystals (0.089 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05728712 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-1251e1d4efb04be2a0db094b4b863a07 |
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| 出典メモ | uspto-grants-1998_03 |
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