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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1260621생성일: 2026년 10월 23일

Methyl iodide → 2-Ethyl-1H-pyrrolo(2,3-b)pyridine

https://huagongshe.com/ko/reaction/1260621

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물2-Methyl-7-azaindoleHCID 583066—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물2-Ethyl-1H-pyrrolo(2,3-b)pyridineHCID 589377—

반응 단계

To a solution of 2-methyl-7-azaindole (1.32 g, 10 mmol) in dry diethyl ether (60 ml) at room temperature under an inert atmosphere is added n-BuLi (18.8 ml of a 1.6 M solution in hexanes, 30 mmol) followed by f-BuOK (2.24 g, 20 mmol). The reaction mixture is stirred at room temperature for 40 minutes and then cooled to −70° C. whereupon methyl iodide (1.25 ml, 20 mmol) is added dropwise. Stirring continues for a further 2 hours after which time, the reaction mixture is quenched with water (2 ml) and is allowed to slowly warm to room temperature. The cooled solution is poured onto water (200 ml), neutralized with 1N HCl and then extracted with diethyl ether (80 ml). The organic portion is washed with water (2×60 ml), dried (Na2SO4) and concentrated in vacuo to yield the titled compound as orange crystals. [MH+CH3CN]+=188)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08470848B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-070eb6e881b445dea67fb75ec5436e14
출처 메모uspto-grants-2013_06