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Dimedone → 3-Acetylamino-5-[(4,6-dimethoxypyrimidin-2yl)oxy]-2-methylindol-4-carboxylic Acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimedone | HCID 31358 | — |
| 反応物 | Allyl 3-Acetylamino-5-[(4,6-dimethoxypyrimidin-2-yl)oxy]-2-methylindol-4-carboxylate | HCID 19962751 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-Acetylamino-5-[(4,6-dimethoxypyrimidin-2yl)oxy]-2-methylindol-4-carboxylic Acid | HCID 19962754 | 93% |
反応手順
0.49 g of allyl 3-acetylamino-5-[(4,6-dimethoxypyrimidin-2-yl)oxy]-2-methylindol-4-carboxylate was dissolved in 10 ml of tetrahydrofuran, and 0.1 g of dimedone and 0.01 g of tetrakistriphenylphosphine palladium were added thereto. The mixture was stirred at room temperature for 4 hours. Crystals obtained by concentration under reduced pressure, was washed with isopropyl ether to obtain 0.41 g (yield: 93%) of the desired compound. mp: 230°-233° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05616537 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-d8978749e11948fcb45208fd1bc39b1f |
| 出典メモ | uspto-grants-1997_04 |