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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 891000생성일: 2026년 10월 25일

Ethyl Bromide → HCID 13006214, 화합물

https://huagongshe.com/reaction/891000

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물1H-Pyrrolo(2,3-b)pyridineHCID 9222—
반응물2,3-Dibromo-N-methylmaleimideHCID 18155—
반응물Ammonium ChlorideHCID 25517—
반응물MagnesiumHCID 5462224—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물HCID 13006214HCID 13006214—
생성물HCID 178418443HCID 178418443—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07001906B2
출처 데이터셋uspto-grants-2006_02
ORD IDord-f2c7b550815040e98b849e8a6a3f822c
출처 메모uspto-grants-2006_02