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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

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物N-(2-(diethylamino)ethyl)-5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxamideHCID 20761785—
反応物5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)indolin-2-oneHCID 21931486—
溶媒EthanolHCID 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-carboxamideHCID 9041714457.4%

反応条件

温度80 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09227962B2
出典データセットuspto-grants-2016_01
ORD IDord-d8b16a692ae744fdacaab30799d055d8
出典メモuspto-grants-2016_01