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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60846생성일: 2026년 10월 24일

2-Amino-5-fluoropyridine → rac-cis-(2-(((5-Fluoropyridin-2-yl)amino)methyl)-3-methylpiperidin-1-yl)(5-(4-fluorophenyl)-2-methylthiazol-4-yl)methanone

https://huagongshe.com/ko/reaction/60846

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-5-fluoropyridineHCID 2737701—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물rac-cis-1-(5-(4-Fluorophenyl)-2-methylthiazole-4-carbonyl)-3-methylpiperidine-2-carbaldehydeHCID 131737135—
용매Ethyl AcetateHCID 8857—
용매Sodium BicarbonateHCID 516892—
용매Acetic acid methanolHCID 10129899—
생성물rac-cis-(2-(((5-Fluoropyridin-2-yl)amino)methyl)-3-methylpiperidin-1-yl)(5-(4-fluorophenyl)-2-methylthiazol-4-yl)methanoneHCID 131737136—

반응 단계

To a stirred solution of rac-cis-1-(5-(4-fluorophenyl)-2-methylthiazole-4-carbonyl)-3-methylpiperidine-2-carbaldehyde and 5-fluoropyridin-2-amine in methanol/acetic acid (50:1) was added sodium cyanoborohydride at 0° C. The reaction was then stirred at rt overnight. After ˜16 h, the reaction mixture was transferred to a seperatory funnel, diluted with EtOAc, saturated NaHCO3 and the layers separated. The organic layer was washed with water, brine, dried (MgSO4), and concentrated in vacuo. The crude reaction mixture was purified by reverse-phase preparative HPLC to afford the title compound. MS (ESI) 443.2 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440982B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-dbdb52e682a049b0969c0e448bb73064
출처 메모uspto-grants-2016_09