関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Boric Acid | HCID 7628 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 3-Bromo-7-hydroxy-4-methylchromen-2-one | HCID 5337545 | — |
| 触媒 | HCID 178418397 | HCID 178418397 | — |
| 生成物 | 6-Hydroxy-2-oxo-1,2-dihydroquinoline-5-carbaldehyde | HCID 86683429 | 42% |
反応手順
Compound 1 (15 g, 46 mmol), the boric acid (8.7 g, 50.6 mmol), Pd(PPh3)4 (1.88 g, 2.3 mmol), Na2CO3 (12.1 g, 115 mmol) were added to DMF (250 mL). The reaction mixture was degassed with N2 for three times, and then heated to 90° C. for 16 h. After cooled to RT, the solvent was concentrated, the residue was dissolved in sat Na2CO3 (150 mL). The aqueous was washed with DCM (100 mL×4), and then acidified by con.HCl to pH to ˜4. The result precipitate was collected by filtration, triturated with hot EA (50 mL), afforded compound 2 (6.5 g, 42%) as yellow solid. 1HNMR (DMSO-d6, 400 MHz): δ 10.55 (s, 1H), 7.71 (d, J=4.0 Hz, 1H), 7.24 (s, 1H), 7.19 (d, J=4.0 Hz, 1H), 6.86 (s, 1H), 3.88 (s, 3H), 2.45 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09040714B2 |
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| 出典データセット | uspto-grants-2015_05 |
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| ORD ID | ord-fd2c5cdf448a4fdaaf8662ae7684b07b |
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| 出典メモ | uspto-grants-2015_05 |
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