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Dimethylformamide → 6-[(E)-2-(dimethylamino)vinyl]-5-nitropyrimidine-2,4-diol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 6-Methyl-5-nitrouracil | HCID 85523 | — |
| 生成物 | 6-[(E)-2-(dimethylamino)vinyl]-5-nitropyrimidine-2,4-diol | HCID 5816188 | 66% |
反応手順
The procedure was adapted from that reported J. Org. Chem. 1978, 43, 2536. Dimethylfomamide-dimethyl acetal (4 mL, 30.05 mmol) was added to a warmed) (80° suspension of 6-methyl-5-nitropyrimidine-2,4(1H,3H)-dione (3 g, 17.54 mmol) in dimethylformamide (10 ml). The resultant mixture was heated to 140° for 30 min then allowed to cool to room temperature. The solid was collected by filtration and washed with ethyl acetate then dried in vacuo to afford 6-[(e)-2-(dimethylamino)vinyl]-5-nitropyrimidine-2,4(1H,3H)-dione (2.62 g, 66%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08765755B2 |
| 出典データセット | uspto-grants-2014_07 |
| ORD ID | ord-2ca71096589b41558dd49c34a5b7f392 |
| 出典メモ | uspto-grants-2014_07 |