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HRID 241730作成日:2026年10月27日

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

https://huagongshe.com/reaction/241730

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-AminobenzonitrileHCID 13396—
反応物Ethyl (methylthio)acetateHCID 78199—
反応物Tert-Butyl hypochloriteHCID 521297—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物3-(Methylsulfanyl)-2-oxo-2,3-dihydro-1H-indole-5-carbonitrileHCID 12351490—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653073B2
出典データセットuspto-grants-2014_02
ORD IDord-2734da931a9542f6aefe4447d2d999b5
出典メモuspto-grants-2014_02