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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 221622생성일: 2026년 10월 25일

1,2-Dichloroethane → 7-bromo-1-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)-2-(chloromethyl)-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/221622

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물Sodium BicarbonateHCID 516892—
반응물Ethyl 2-chloroethanecarboximidate hydrochlorideHCID 12470659—
반응물7-bromo-N4-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)quinoline-3,4-diamineHCID 69105440—
용매ChloroformHCID 6212—
생성물7-bromo-1-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)-2-(chloromethyl)-1H-imidazo[4,5-c]quinolineHCID 67157483—

반응 조건

온도70 °C

반응 단계

A 1-L, three-necked, Morton flask, equipped with overhead stirrer, was charged with 7-bromo-N4-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)quinoline-3,4-diamine (33.4 g, 81.0 mmol) and 1,2-dichloroethane (400 mL) and the mixture was stirred under N2. Ethyl 2-chloroethanimidoate hydrochloride (29.1 g, 184.0 mmol) was then added in portions and the reaction mixture was heated to 70° C. for 3 days. The reaction mixture was then cooled to ambient temperature and treated with CHCl3 (500 mL) and saturated aqueous NaHCO3 solution (700 mL). The layers were separated and the organic portion was concentrated under reduced pressure to give 38 g of 7-bromo-1-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)-2-(chloromethyl)-1H-imidazo[4,5-c]quinoline as a golden solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207162B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-981adcc57ad14a6dacdb6502098b97d2
출처 메모uspto-grants-2012_06