関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2,4-Dimethoxybenzoyl chloride | HCID 2734719 | — |
| 反応物 | 1-Piperidin-4-yl-1,3-dihydro-2H-indol-2-one | HCID 2761152 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 1-(1-(2,4-Dimethoxybenzoyl)-4-piperidyl)indol-2-one | HCID 22914657 | 45.1% |
反応手順
1-(4-Piperidyl)indol-2-one (53 mg, 0.245 mmole), 2,4-dimethoxybenzoyl chloride (54 mg, 0.27 mmole), and 38 mL (0.27 mmole) triethylamine were mixed in 4 ml of chloroform at 0° C. The reaction mixture was stirred at 0° C. for 5 minutes and then at 23° C. for 15 minutes during which time the pH was adjusted to 7.5 with triethylamine. The reaction mixture was concentrated under reduced pressure and the residue was purified by preparative thick layer chromatography (CHCl3 --CH3OH--NH4OH; 95:5:0.5) to yield 42 mg of the title compound: m.p. 88°-93° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05665719 |
|---|
| 出典データセット | uspto-grants-1997_09 |
|---|
| ORD ID | ord-75a0481253b94f3ea3f76576417ad1fe |
|---|
| 出典メモ | uspto-grants-1997_09 |
|---|