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HRID 891000作成日:2026年10月26日

Ethyl Bromide → HCID 13006214、化合物

https://huagongshe.com/reaction/891000

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl BromideHCID 6332—
反応物1H-Pyrrolo(2,3-b)pyridineHCID 9222—
反応物2,3-Dibromo-N-methylmaleimideHCID 18155—
反応物Ammonium ChlorideHCID 25517—
反応物MagnesiumHCID 5462224—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 13006214HCID 13006214—
生成物HCID 178418443HCID 178418443—

反応手順

A solution of ethylmagnesium bromide is prepared, starting from magnesium (12.7 mmol) suspended in bromoethane (12.7 mmol) and dry tetrahydrofuran (5 ml). The solution is stirred at ambient temperature for 1 hour and then 7-azaindole (12.7 mmol), dissolved in 40 ml of anhydrous toluene, is added dropwise. After stirring at ambient temperature for 1 hour 30 minutes, a solution of N-methyl-2,3-dibromomaleimide (3.53 mmol) in 40 ml of anhydrous toluene is added dropwise. After 20 minutes, 60 ml of dry dichloromethane are added; the reaction mixture is then stirred at 40° C. for 75 hours and hydrolysed with saturated aqueous ammonium chloride solution. The organic product is extracted with ethyl acetate, and the organic phases are then combined, dried over magnesium sulphate and filtered. After evaporating off the solvent and purifying the residue by chromatography on silica gel (cyclohexane/ethyl acetate: 3/2), the expected product is isolated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07001906B2
出典データセットuspto-grants-2006_02
ORD IDord-f2c7b550815040e98b849e8a6a3f822c
出典メモuspto-grants-2006_02