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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 852108생성일: 2026년 10월 25일

4-Benzylpiperidine → (S)-1-(4-benzyl-piperidin-1-yl)-3-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-phenoxy]-propan-2-ol

https://huagongshe.com/reaction/852108

반응식

참여 물질

역할이름HCID투입량
반응물4-BenzylpiperidineHCID 31738—
반응물(S)-6-fluoro-3-(4-oxiranylmethoxy-phenyl)-benzo[d]isoxazoleHCID 11254641—
용매EthanolHCID 702—
용매DimethylformamideHCID 6228—
생성물(S)-1-(4-benzyl-piperidin-1-yl)-3-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-phenoxy]-propan-2-olHCID 982550770%

반응 조건

온도85 °C

반응 단계

Combine (S)-6-fluoro-3-(4-oxiranylmethoxy-phenyl)-benzo[d]isoxazole (150 mg, 0.526 mmol) dissolved in dimethylformamide (˜2 mL) and add 0.13 M solution of 4-benzylpiperidine in ethanol (˜4 mL) and heat for 10 hours at 85° C. Concentrate and purify the reaction mixture by flash (silica) chromatography on a Water's Sep-Pak 5 g silica cartridge using a graded solvent mixture of dichloromethane to 10% methanol in dichloromethane to give the title compound (169.9 mg, 70% Yield). Purity by LC/MS=99%, [M+H]+=461.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07253165B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-099d0be113d54634872c63a608134850
출처 메모uspto-grants-2007_08