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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62246생성일: 2026년 10월 24일

p-Toluenesulfonic acid → (E)-6-methoxy-5-morpholino-2-((6-(trifluoromethyl)pyridin-3-yl)methylene)-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/ko/reaction/62246

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물6-(Trifluoromethyl)pyridine-3-carboxaldehydeHCID 2777762—
반응물6-Methoxy-5-morpholino-2,3-dihydro-1H-inden-1-oneHCID 117940128—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물(E)-6-methoxy-5-morpholino-2-((6-(trifluoromethyl)pyridin-3-yl)methylene)-2,3-dihydro-1H-inden-1-oneHCID 117940111—

반응 조건

온도120 °C

반응 단계

To a solution of 13 (100 mg, 0.404 mmol) in toluene 5 ml was added 6-(trifluoromethyl) nicotinaldehyde 69 (70.8 mg, 0.404 mmol). PTSA (154 mg, 0.808 mmol) was added, and the reaction mixture stirred at 120° C. for 6 h. The reaction mass was diluted with ethyl acetate and washed with water (3×25 mL). The organic layer was dried over sodium sulphate and concentrated to get the crude compound (E)-6-methoxy-5-morpholino-2-((6-(trifluoromethyl)pyridin-3-yl)methylene)-2,3-dihydro-1H-inden-1-one 70. The crude 70 was purified through flash chromatography by using 100-200 mesh silica gel. The compound was eluted at 32% ethyl acetate in hexane to afford yellow coloured solid 70.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09446047B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-59fda7acb3144c72ab068759e0d0d8c1
출처 메모uspto-grants-2016_09