関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | 3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-one | HCID 70979018 | — |
| 生成物 | 3-(4-(Tert-butyl)phenyl)-1-chloro-6-methoxyisoquinoline | HCID 86683269 | 28% |
反応手順
A solution of 3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-one (0.7 g, 2.277 mmol) in POCl3 (7 ml) was refluxed for overnight. The solvent was evaporated under reduced pressure and the residue was diluted with cold water. The aqueous solution was basified by solid sodium carbonate and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to get crude compound. The crude compound was purified by silica gel chromatography (10% ethyl acetate in pet ether) to get desired compound (0.21 g, 28.0%) as solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 8.34(s, 1H), 8.18-8.16 (d, J=8 Hz, 1H), 8.08-8.06 (d, J=8 Hz, 2H), 7.57-7.55 (d, J=8 Hz, 2H), 7.41 (s, 1H), 7.40-7.38 (d, J=8 Hz, 1H), 3.97 (s, 3H), 1.34 (s, 9H); MS: MS m/z 362.2 (M++1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08957203B2 |
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| 出典データセット | uspto-grants-2015_02 |
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| ORD ID | ord-c0a156650a184eb2bbb2c3f68ed63fbc |
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| 出典メモ | uspto-grants-2015_02 |
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