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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1160206생성일: 2026년 10월 27일

Acetic Acid → 1-(4-Fluoro-phenyl)-2-[4(pyrazin-2-yloxy)-benzyl amino]-ethanol

https://huagongshe.com/reaction/1160206

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물2-Amino-1-(4-fluorophenyl)ethan-1-olHCID 9827—
반응물4-(Pyrazin-2-yloxy)benzaldehydeHCID 3614411—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
생성물1-(4-Fluoro-phenyl)-2-[4(pyrazin-2-yloxy)-benzyl amino]-ethanolHCID 6843303235.1%

반응 단계

Sodium cyanoborohydride (0.62 mL, 1 M in THF) was added to a solution of 2-amino-1-(4-fluoro-phenyl)-ethanol (80 mg, 0.52 mmol), 4-(Pyrazin-2-yloxy)-benzaldehyde (103 mg, 0.52 mmol) and glacial acetic acid (0.5 mL), in methanol (3 mL) at RT and the flask was stirred overnight. The reaction mixture was concentrated in vacuo; the residue was quenched with saturated aqueous sodium bicarbonate solution and then extracted with dichloromethane (3×4 mL). The combined organic phases were dried over anhydrous sodium sulfate and concentrated again in vacuo to yield 1-(4-fluoro-phenyl)-2-[4(pyrazin-2-yloxy)-benzyl amino]-ethanol as a white solid 62 mg, 35%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07816354B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-5785338dbe8142e1ae257bab1d2179f2
출처 메모uspto-grants-2010_10