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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 564084생성일: 2026년 10월 27일

4-Benzyloxy-1-{2-oxo-2-[3-(2,2,2-trifluoro-acetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-ethyl}-1H-pyridin-2-one → 4-Hydroxy-1-{2-[3-(2,2,2-trifluoro-acetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-ethyl}-1H-pyridin-2-one

https://huagongshe.com/reaction/564084

반응식

참여 물질

역할이름HCID투입량
반응물4-Benzyloxy-1-{2-oxo-2-[3-(2,2,2-trifluoro-acetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-ethyl}-1H-pyridin-2-oneHCID 58042874—
촉매PalladiumHCID 23938—
용매Hydrochloric AcidHCID 313—
용매MethanolHCID 887—
생성물4-Hydroxy-1-{2-[3-(2,2,2-trifluoro-acetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-ethyl}-1H-pyridin-2-oneHCID 59822086—

반응 조건

온도50 °C

반응 단계

To 5.00 g (10.3 mmol) 4-benzyloxy-1-{2-oxo-2-[3-(2,2,2-trifluoro-acetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-ethyl}-1H-pyridin-2-one (preparation 21a) in 100 mL MeOH and 9.8 mL 1 M aqueous HCl-solution is added 500 mg of 10% Pd/C. The reaction mixture is stirred under a hydrogen atmosphere of 5000 hPa at 50° C. for 18 h. After filtration and evaporation of the solvent, is the residue purified by HPLC (Zorbax stable bond, C18; water (0.15% formic acid)/acetonitrile 95:5 to 5:95).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067590B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-e646eb6962724d7cb52170bde82d6f38
출처 메모uspto-grants-2011_11