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HRID 2379487作成日:2026年10月26日

Dicyclohexylcarbodiimide → 3-(3,5-Di-tert-butyl-4-hydroxycinnamoylamino)-4-(2-chlorophenyl)-6,8-dimethylquinoline

https://huagongshe.com/reaction/2379487

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物3-(3,5-Ditert-butyl-4-hydroxyphenyl)prop-2-enoic acidHCID 99819—
反応物3-Amino-4-(2-chlorophenyl)-6,8-dimethylquinolineHCID 10446536—
溶媒DimethylformamideHCID 6228—
生成物3-(3,5-Di-tert-butyl-4-hydroxycinnamoylamino)-4-(2-chlorophenyl)-6,8-dimethylquinolineHCID 5379890147.5%

反応手順

1-Hydroxybenzotriazole (154 mg) and dicyclohexylcarbodiimide (272 mg) were added to a solution of 3,5-di-tert-butyl-4-hydroxycinnamic acid (331 mg) in DMF (5 ml). The mixture was stirred at room temperature for minutes, and then, 3-amino-4-(2-chlorophenyl)-6,8-dimethylquinoline (288 mg) was added thereto. The resultant mixture was further stirred at room temperature for 24 hours. The insoluble materials were filtered off, while the filtrate was diluted with water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4). The solvent was removed, and the residue was purified by a silica gel chromatography with benzene-acetone (9:1), then, crystallized from isopropyl ether to give 3-(3,5-di-tert-butyl-4-hydroxycinnamoylamino)-4-(2-chlorophenyl)-6,8-dimethylquinoline (257 mg, 47.5%) as colorless needles.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05362742
出典データセットuspto-grants-1994_11
ORD IDord-98e97a8dae82496c9ce64dca0b50cc24
出典メモuspto-grants-1994_11