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HRID 2079145생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2079145

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—
반응물2-{3-[(4-carbamimidoylphenylamino)-(2-fluoro-4,5-dimethoxyphenyl)methyl]5-oxo-4,5-dihydro-[1,2,4]triazol-1-yl}benzoic Acid TrifluoroacetateHCID 136337083—
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], 1g 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 번호US07928228B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-010dfd1d80a64cc7bc8e13e0d15a4805
출처 메모uspto-grants-2011_04