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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 254014생성일: 2026년 10월 25일

1-Butanaminium, N,N,N-tributyl-, fluoride, hydrate → N,N-di(1,1-dimethylethoxycarbonyl)-3-(1-(2,3-difluorophenyl)-1H-tetrazol-5-yl)-5-ethynylpyridin-2-amine

https://huagongshe.com/reaction/254014

반응식

참여 물질

역할이름HCID투입량
반응물1-Butanaminium, N,N,N-tributyl-, fluoride, hydrateHCID 16211673—
반응물N,N-di(1,1-dimethylethoxycarbonyl)-3-(1-(2,3-difluorophenyl)-1H-tetrazol-5-yl)-5-(2-(trimethylsilyl)ethynyl)pyridin-2-amineHCID 58179633—
용매DichloromethaneHCID 6344—
생성물N,N-di(1,1-dimethylethoxycarbonyl)-3-(1-(2,3-difluorophenyl)-1H-tetrazol-5-yl)-5-ethynylpyridin-2-amineHCID 5818003383.3%

반응 조건

온도0 °C

반응 단계

N,N-Di(1,1-dimethylethoxycarbonyl)-3-(1-(2,3-difluorophenyl)-1H-tetrazol-5-yl)-5-(2-(trimethylsilyl)ethynyl)pyridin-2-amine (713 mg, 1.2 mmol) was dissolved in methylene chloride (10 mL) and cooled to 0° C. To this was added tetrabutylammonium fluoride hydrate (163 mg, 625 μmol) in methylene chloride (1 mL). The reaction was loaded directly onto silica and chromatographed (10% ethyl acetate/hexane to 50% ethyl acetate/hexane) to give N,N-di(1,1-dimethylethoxycarbonyl)-3-(1-(2,3-difluorophenyl)-1H-tetrazol-5-yl)-5-ethynylpyridin-2-amine (496 mg, 1.0 mmol, 83%) as a yellow solid; 1H NMR (CDCl3): 1.37 (s, 18H), 3.35 (s, 1H), 7.30 (m, 1H), 7.40 (m, 2H), 7.89 (s, 1H), 8.75 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872031B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-7b3de68b84d94b51b0d667bcb3a66dde
출처 메모uspto-grants-2011_01