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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 908930생성일: 2026년 10월 24일

4-Methylmorpholine → 2-(4-Dimethylamino-4-phenylcyclohexylidene)-N-(4-fluoro-phenyl)acetamide

https://huagongshe.com/ko/reaction/908930

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물4-FluoroanilineHCID 9731—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Sodium HydroxideHCID 14798—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물(4-Dimethylamino-4-phenylcyclohexylidene)acetic acid hydrochlorideHCID 67386703—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(4-Dimethylamino-4-phenylcyclohexylidene)-N-(4-fluoro-phenyl)acetamideHCID 1153833182%

반응 조건

온도0 °C

반응 단계

1-Hydroxybenzotriazole (273 mg, 2.0 mmol), 4-fluoroaniline (0.095 ml, 1.0 mmol) and N-methylmorpholine (0.222 ml, 2.0 mmol) were added to a solution of (4-dimethylamino-4-phenylcyclohexylidene)acetic acid hydrochloride (296 mg, 1.0 mmol) in dry dimethylformamide (10 ml) under argon. The solution was cooled to 0° C. and dicyclohexylcarbodiimide (417 mg, 2.0 mmol) was added. The reaction mixture was stirred at RT for 7 d. Working up of the mixture was carried out by separating off the urea which had precipitated out and introducing the filtrate into a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml). Still further urea thereby precipitated out and was separated off. 5 M sodium hydroxide solution (4 ml, 20 mmol) was added to the aqueous phase and the mixture was diluted with water (300 ml) and stored at 5° C. for 3 d. The product thereby precipitated out as a colourless solid in a yield of 82% (287 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08017630B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-829042f2a02e4e5a8c922df054972f75
출처 메모uspto-grants-2011_09