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Acetylpyrazine → (E)-3-(Dimethylamino)-1-(pyrazin-2-YL)prop-2-EN-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetylpyrazine | HCID 30914 | — |
| 反応物 | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 溶媒 | tert-Butyl methyl ether | HCID 15413 | — |
| 生成物 | (E)-3-(Dimethylamino)-1-(pyrazin-2-YL)prop-2-EN-1-one | HCID 5825354 | 81.4% |
反応手順
A solution of acetylpyrazine (5 g, 40.9 mmol) in N,N-dimethylformamide dimethyl acetal (10.9 mL, 81.8 mmol) and Et3N (5.7 mL) was heated at 110° C. for 16 h. The heating was stopped and a precipitate was formed while it was allowed to cool down to room temperature. The suspension was diluted with tert-butyl methyl ether; the solid was separated by filtration and washed with tert-butyl methyl ether. This material was triturated with the same solvent, filtered off and dried to afford the title compound 23a as a yellow solid (5.9 g, 33.3 mmol, 81% yield). 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.09 (s, 1H), 8.73 (d, J=2.4 Hz, 1H), 8.66 (dd, J=2.4, 1.6 Hz, 1H), 7.84 (d, J=12.4 Hz, 1H), 6.30-6.20 (m, 1H), 3.19 (s, 3H), 2.93 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08088805B2 |
| 出典データセット | uspto-grants-2012_01 |
| ORD ID | ord-fc1dd4dd780c44d7b0412d37f347e4b9 |
| 出典メモ | uspto-grants-2012_01 |