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HRID 241730생성일: 2026년 10월 26일

Triethylamine → 3-(Methylsulfanyl)-2-oxo-2,3-dihydro-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/241730

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-AminobenzonitrileHCID 13396—
반응물Ethyl (methylthio)acetateHCID 78199—
반응물Tert-Butyl hypochloriteHCID 521297—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물3-(Methylsulfanyl)-2-oxo-2,3-dihydro-1H-indole-5-carbonitrileHCID 12351490—

반응 단계

To a solution of 4-amino-benzonitrile (84.64 mmoles) in DCM (200 ml) under a nitrogen atmosphere, at −78° C., there is added, dropwise, tBuOCl (84.64 mmoles) dissolved in 20 ml of DCM and then, after 10 minutes, ethyl (methylsulphanyl)acetate (84.64 mmoles) dissolved in 20 ml of DCM is added dropwise to the reaction mixture. After stiffing for one hour at −78° C., triethylamine (0.152 mol) is added dropwise. The reaction mixture is stirred at ambient temperature for one hour. Water is added and the phases are then separated. The organic phase is washed with water and then with saturated aqueous NaCl solution. The organic phase is dried over sodium sulphate, filtered and evaporated to dryness. The residue is taken up in ethyl ether and aq. 2M HCl solution is added. After stiffing overnight, the yellow precipitate is filtered off and dried in vacuo to yield the title product, which is used directly in the next reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653073B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-2734da931a9542f6aefe4447d2d999b5
출처 메모uspto-grants-2014_02