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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 340665생성일: 2026년 10월 25일

Triethylamine → N-(4-Hydroxy-3-oxo-2,3-dihydro-1H-inden-5-yl)-5-phenylpentanamide

https://huagongshe.com/reaction/340665

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzenepentanoic acidHCID 16757—
반응물Diethyl cyanophosphonateHCID 76257—
반응물6-Amino-7-hydroxy-2,3-dihydro-1H-inden-1-one hydrobromideHCID 67353461—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물N-(4-Hydroxy-3-oxo-2,3-dihydro-1H-inden-5-yl)-5-phenylpentanamideHCID 5778127926.3%

반응 단계

6-Amino-7-hydroxyindan-1-one hydrobromide (50 mg, 0.256 mmol) and 5-phenylvaleric acid (54.8 mg, 0.307 mmol) were dissolved in N,N-dimethylformamide (1.3 mL), diethyl cyanophosphate (45.7 μL, 0.307 mmol) and triethylamine (120 μL, 0.896 mmol) were added, and the mixture was stirred at room temperature for 15 min. The reaction solution was diluted with diethyl ether, washed with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=10/90→40/60) to give the title compound (21.8 mg, yield 26%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895591B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-1686fa72340c4af39303b86535ea67a8
출처 메모uspto-grants-2014_11