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Water → 4-[3-(4-Oxo-4,5,6,7-tetrahydroindolon-1-yl)propionylamino} Benzoic Acid Ethyl Ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Ethyl 4-[(1-oxoallyl)amino]benzoate | HCID 84618 | — |
| 反応物 | 1,5,6,7-Tetrahydro-4H-indol-4-one | HCID 280229 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-[3-(4-Oxo-4,5,6,7-tetrahydroindolon-1-yl)propionylamino} Benzoic Acid Ethyl Ester | HCID 86586941 | 56% |
反応手順
In the second step, 4-acryloylaminobenzoic acid ethyl ester (200 mg, 0.91 mmol), 1,5,6,7-tetrahydro-4H-indol-4-one (123 mg, 0.91 mmol) and potassium carbonate (126 mg, 0.91 mmol) were combined in dry N,N-dimethylformamide (3 mL) and stirred at room temperature for 24 hours, then heated to 60 C for 6 hours. Water (20 mL) was added and the resulting precipitate was vacuum filtered washing with water. The isolated solid was dried under vacuum to yield 180 mg (56%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08377456B2 |
| 出典データセット | uspto-grants-2013_02 |
| ORD ID | ord-ffff7568472e4ea0b5c9df2a1a17fbfc |
| 出典メモ | uspto-grants-2013_02 |