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HRID 1698665생성일: 2026년 10월 26일

Trimethylsilyl cyanide → (8-Methoxychroman-6-yl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrile

https://huagongshe.com/reaction/1698665

반응식

참여 물질

역할이름HCID투입량
반응물Trimethylsilyl cyanideHCID 82115—
반응물Ytterbium triflateHCID 2733225—
반응물8-Methoxychromane-6-carbaldehydeHCID 12831983—
반응물4-(5-Methyl-1,2,4-oxadiazol-3-yl)anilineHCID 18188176—
용매DichloromethaneHCID 6344—
생성물(8-Methoxychroman-6-yl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrileHCID 67097438—

반응 단계

After adding 700 mg of 4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamine, 770 mg of 8-methoxychromane-6-carbaldehyde [CAS No. 81258-23-3], 1 g of MS3A and 1.1 ml of trimethylsilyl cyanide to a solution of 250 mg of Yb(OTf)3 in 5 ml of dichloromethane under a nitrogen atmosphere, the mixture was stirred overnight at room temperature. The reaction mixture was filtered through celite, and the celite was washed with 100 ml of ethyl acetate. The organic layer was concentrated under reduced pressure to give a crude product of (8-methoxychroman-6-yl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08163787B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-72202eace7bb4f4284da39978a7dbac8
출처 메모uspto-grants-2012_04