関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Methyl 3,5-dimethoxyphenylacetate | HCID 592191 | — |
| 反応物 | 6-Chloro-4-(methylamino)nicotinaldehyde | HCID 23434571 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 7-chloro-3-(3,5-dimethoxyphenyl)-1-methyl-1,6-naphthyridin-2(1H)-one | HCID 86713576 | 80.8% |
反応手順
A mixture of 6-chloro-4-(methylamino)nicotinaldehyde (3.7 g, 21.7 mmol), methyl 2-(3,5-dimethoxyphenyl)acetate (4.5 g, 21.7 mmol) and potassium carbonate (9.0 g, 65.1 mmol) in N,N-dimethylformamide (30 mL) was heated at 105° C. for 5 h. LCMS showed the reaction was completed. The reaction was cooled to RT, quenched with water (200 mL), and filtered. The filtration cake was washed by petroleum ether (50 mL) and ethyl acetate (50 mL) to afford the title compound (5.8 g, 77%) as a yellow solid. MS (ES+) C18H19ClN2O3 requires: 346, 348. found: 347, 349 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09340514B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-9cf9ea22fa634854a14f4dd1149174fa |
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| 出典メモ | uspto-grants-2016_05 |
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