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2,2-Dimethoxy-1-methylpyrrolidine → 1-(4-Methoxyphenyl)-3-(1-methyl-2-pyrrolidinylidene)-2(1H,3H)-indolone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,2-Dimethoxy-1-methylpyrrolidine | HCID 11073552 | — |
| 反応物 | 1-(4-Methoxyphenyl)-1,3-dihydro-2H-indol-2-one | HCID 13339544 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 1-(4-Methoxyphenyl)-3-(1-methyl-2-pyrrolidinylidene)-2(1H,3H)-indolone | HCID 54126479 | — |
反応手順
1-(4-Methoxyphenyl)-2(1H,3H)-indolone (49 g, 0.205 mole), N-methyl-2-pyrrolidone dimethyl acetal (ca. 80%, 53 g, 0.245 mole, Ber, 97, pp. 3081-7, 1964) and 1000 ml chloroform were refluxed under nitrogen for 1.5 hours. The reaction mixture was cooled and evaporated in vacuo to solids. Two recrystallizations from ethyl acetate gave purified title product, 44.7 g, m.p. 90°-93° C. Thirty grams of this material were dried at 80° C./15 mm Hg for 20 hours to give 26.1 g of title product, m.p. 127°-9° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04879391 |
| 出典データセット | uspto-grants-1989_11 |
| ORD ID | ord-8d039b96c52c4204babea6ff1ea17f6c |
| 出典メモ | uspto-grants-1989_11 |