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HRID 1818045作成日:2026年10月27日

Piperidine → (E,E)-2-(Benzylaminocarbonyl)-3-(4-hydroxy-3-methoxystyryl)acrylonitrile

https://huagongshe.com/reaction/1818045

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)-HCID 9984—
反応物N-(cyanoacetyl)benzylamideHCID 178511179—
溶媒EthanolHCID 702—
生成物(E,E)-2-(Benzylaminocarbonyl)-3-(4-hydroxy-3-methoxystyryl)acrylonitrileHCID 11522842—

反応手順

The compound was prepared as described in Example 37 by adding piperidine to a solution of 4-hydroxy-3-methoxycinnamaldehyde (35 mg, 0.2 mmol) and N-(cyanoacetyl)benzylamide (34 mg, 0.2 mmol) in ethanol. After recrystallization from ethanol-water a yellow solid was obtained (50 mg, 75%). The product gave the following analytical data:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07598419B2
出典データセットuspto-grants-2009_10
ORD IDord-1076ebe740ce40c7a1d72d72c5535048
出典メモuspto-grants-2009_10