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Triethylamine → 5-(Dimethylaminomethylenamino)-3-(4-quinolylmethylen)-2-oxindole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 5-Amino-3-(quinol-4-ylmethylene)-2-oxindole | HCID 54536702 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-(Dimethylaminomethylenamino)-3-(4-quinolylmethylen)-2-oxindole | HCID 54093817 | 60% |
反応手順
To a solution of 5-amino-3-(4-quinolylmethylen)-2-oxindole (287 mg, 1 mmol) and triethylamine (121 mg, 1.2 mmol) in THF (20 ml) was added portionwise at, 0° C. chlorodimethyl-formimminium chloride (154 mg, 1.2 mmol) and the stirring was continued at room temperature for 1 h. Then the reaction mixture was diluted with dichloromethane, the organic layer washed with brine, dried over sodium sulfate and concentrated under vacuum. The residue was chromatographed on silica gel (eluant ethyl acetate/methanol 1:1) to give pure title compound in 60% yield (205 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05905149 |
| 出典データセット | uspto-grants-1999_05 |
| ORD ID | ord-b987982202434f22b89e60cb640d9d6a |
| 出典メモ | uspto-grants-1999_05 |