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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353596생성일: 2026년 10월 25일

Acetic Acid → (2-(4-((6-Quinolylamino)methyl)phenoxy)ethyl)diethylamine

https://huagongshe.com/reaction/353596

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물6-AminoquinolineHCID 11373—
반응물Sodium HydroxideHCID 14798—
반응물4-(2-(Diethylamino)-Ethoxy)-BenzaldehydeHCID 411674—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
생성물(2-(4-((6-Quinolylamino)methyl)phenoxy)ethyl)diethylamineHCID 235143838.3%

반응 단계

To a stirred solution of 1.0 gram (0.0045 mole) of 4-(2-(diethylamino)ethoxy)benzaldehyde and 0.65 gram (0.0045 mole) of 6-aminoquinoline (available from Aldrich Chemical Company) in 25 mL of 1,2-dichloroethane (DCE, available from Aldrich Chemical Company) was added 0.3 mL (0.0045 mole) of glacial acetic acid (available from J. T. Baker Inc.) followed by 1.4 grams (0.0068 mole) of sodium triacetoxyborohydride (available from Aldrich Chemical Company). Upon completion of addition, the reaction mixture was stirred at ambient temperature for three hours. At the conclusion of this period, 50 mL of 10% aqueous sodium hydroxide was added dropwise. The resulting solution was extracted with three 25 mL portions of diethyl ether. The extracts were combined, washed with one 25 mL portion of an aqueous solution saturated with sodium chloride, dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 1.25 grams of a dark brown paste. The dark brown paste was purified by column chromatography on silica gel, yielding 0.13 gram of Compound 15. The NMR spectrum was consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06753429B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-fcbe1e5a9d5b42bea75a6652b652f34a
출처 메모uspto-grants-2004_06