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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2379487생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2379487

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-(3,5-Ditert-butyl-4-hydroxyphenyl)prop-2-enoic acidHCID 99819—
반응물3-Amino-4-(2-chlorophenyl)-6,8-dimethylquinolineHCID 10446536—
용매DimethylformamideHCID 6228—
생성물3-(3,5-Di-tert-butyl-4-hydroxycinnamoylamino)-4-(2-chlorophenyl)-6,8-dimethylquinolineHCID 5379890147.5%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05362742
출처 데이터셋uspto-grants-1994_11
ORD IDord-98e97a8dae82496c9ce64dca0b50cc24
출처 메모uspto-grants-1994_11