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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480194생성일: 2026년 10월 25일

N,N-Diethylethylenediamine → (2R,5S)-2-{4-Chloro-2-[(2-diethylamino-ethylamino)-methyl]-phenoxy}-1-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-ethanone

https://huagongshe.com/reaction/480194

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DiethylethylenediamineHCID 60993—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Dichloroethane acetic acidHCID 18768099—
반응물(2R,5S)-5-Chloro-2-{2-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzaldehydeHCID 53673807—
용매WaterHCID 962—
생성물(2R,5S)-2-{4-Chloro-2-[(2-diethylamino-ethylamino)-methyl]-phenoxy}-1-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-ethanoneHCID 1211211230.1%

반응 단계

To a solution of (2R,5S)-5-chloro-2-{2-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzaldehyde (0.100 g, 0.25 mmol) in 10:1 dichloroethane acetic acid (2.2 mL) was added (diethylamino)ethylamine (0.088 mL, 0.625 mmol) and the resulting solution was stirred for 1 hour at ambient temperature. To this was added sodium cyanoborohydride (0.0094 g, 0.15 mmol) and the reaction was stirred overnight at ambient temperature. Upon completion water was added and the mixture was basified with solid sodium bicarbonate (pH>10). The product was extracted with dichloromethane (2×) and diethyl ether (2×). The combined organics were dried over magnesium sulfate, filtered and concentrated in vacuo. Chromatography on silica gel gave the title compound (0.039 g, x 30% yield)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06649611B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-dba56af168444ddabdea68328ee57ade
출처 메모uspto-grants-2003_11