化工社化工社 化学情報印刷レポート · 研究参考用
HRID 588280作成日:2026年10月27日
Piperidine → (Z)-N-(2-(diethylamino)ethyl)-2,4-dimethyl-5-((2-oxo-5-(4,4, 5,5-tetramethyl-1,3,2-dioxab orolan-2-yl)indolin-3-ylidene)methyl)-1H-pyrrole-3-carboxamide
https://huagongshe.com/reaction/588280
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | N-(2-(diethylamino)ethyl)-5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxamide | HCID 20761785 | — |
| 反応物 | 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-2-one | HCID 21931486 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (Z)-N-(2-(diethylamino)ethyl)-2,4-dimethyl-5-((2-oxo-5-(4,4, 5,5-tetramethyl-1,3,2-dioxab orolan-2-yl)indolin-3-ylidene)methyl)-1H-pyrrole-3-carboxamide | HCID 90417144 | 57.4% |
反応手順
To a solution of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-2-one (195 mg, 0.75 mmol) in EtOH (3 ml) was added N-(2-(diethylamino)ethyl)-5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxamide (200 mg, 0.76 mmol) and piperidine (82 μL, 0.83 mmol). The mixture was stirred at 80° C. for 1 hour. After cooled down to room temperature, the reaction mixture was concentrated, filtrated, and washed with EtOH to give (Z)—N-(2-(diethylamino)ethyl)-2,4-dimethyl-5-((2-oxo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-3-ylidene)methyl)-1H-pyrrole-3-carboxamide (218 mg) as yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US09227962B2 |
|---|
| 出典データセット | uspto-grants-2016_01 |
|---|
| ORD ID | ord-d8b16a692ae744fdacaab30799d055d8 |
|---|
| 出典メモ | uspto-grants-2016_01 |
|---|