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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352055생성일: 2026년 10월 26일

Water → Mubritinib

https://huagongshe.com/reaction/352055

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물4-(chloromethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazoleHCID 9857126—
반응물4-(4-[1,2,3]Triazol-1-yl-butyl)phenolHCID 12109494—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물MubritinibHCID 644469293%

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온도70 °C

반응 단계

4-[4-(1H-1,2,3-Triazol-1-yl)butyl]phenol (400 mg, 1.84 mmol) and 4-(chloromethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole (529 mg, 1.84 mmol) were dissolved in dimethylformamide (3 ml) and potassium carbonate (279 mg, 2.02 mmol) was added. The mixture was stirred at 65-75° C. for 4 hours. 4-[4-(1H-1,2,3-Triazol-1-yl)butyl]phenol (40 mg, 0.184 mmol) was added and the mixture was stirred at 65-75° C. for further 3 hours. The mixture was cooled to room temperature and water (5 ml) was added, then methanol (3 ml) was added. The mixture was stirred at room temperature for 40 min, and the precipitated crystals were collected by filtration and washed with water. The crystals were dried under reduced pressure to give 1-[4-[4-[[2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazol-4-yl]methoxy]phenyl]butyl]-1H-1,2,3-triazole (799 mg, yield 93%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743924B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-48ba846d4d674c9ab2d6e54c1c312e97
출처 메모uspto-grants-2004_06