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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1698687생성일: 2026년 10월 27일

Trimethylsilyl cyanide → (5-fluoro-8-methoxy-4H-benzo[1,3]dioxin-6-yl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrile

https://huagongshe.com/reaction/1698687

반응식

참여 물질

역할이름HCID투입량
반응물Trimethylsilyl cyanideHCID 82115—
반응물Ytterbium triflateHCID 2733225—
반응물4-(5-Methyl-1,2,4-oxadiazol-3-yl)anilineHCID 18188176—
반응물5-fluoro-8-methoxy-4H-benzo[1,3]dioxine-6-carbaldehydeHCID 59516817—
용매TetrahydrofuranHCID 8028—
생성물(5-fluoro-8-methoxy-4H-benzo[1,3]dioxin-6-yl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrileHCID 67097262—

반응 단계

To a solution of 45 mg of Yb(OTf)3 in 3 ml of THF there were added 126 mg of 4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamine, 153 mg of 5-fluoro-8-methoxy-4H-benzo[1,3]dioxine-6-carbaldehyde, 0.2 g of MS3A and 192 μl of trimethylsilyl cyanide under a nitrogen atmosphere, and the mixture was stirred overnight at room temperature. The reaction mixture was filtered through celite, and the celite was washed with THF. The organic layer was concentrated under reduced pressure to give (5-fluoro-8-methoxy-4H-benzo[1,3]dioxin-6-yl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrile (crude product).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163787B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-bbb0dc8b082c4369b261440cca9fccd0
출처 메모uspto-grants-2012_04