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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 476166생성일: 2026년 10월 24일

Water → 2-(4-(8-Bromo-3-(2-methyl-5-nitrophenylsulfonyl)-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-1-yl)phenyl)-2-methylpropanenitrile

https://huagongshe.com/ko/reaction/476166

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물o-Toluenesulfonyl chloride, 5-nitro-HCID 8457—
반응물TriethylamineHCID 8471—
반응물4-(8-Bromo-2,3-dihydro-2-oxo-1H-imidazo(4,5-c)quinolin-1-yl)-alpha,alpha-dimethylbenzeneacetonitrileHCID 42609569—
용매DichloromethaneHCID 6344—
생성물2-(4-(8-Bromo-3-(2-methyl-5-nitrophenylsulfonyl)-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-1-yl)phenyl)-2-methylpropanenitrileHCID 66897149—

반응 단계

To a solution of 2-(4-(8-bromo-2-oxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-1-yl)phenyl)-2-methylpropanenitrile (Intermediate 1, 50 mg, 0.12 mmol) and triethylamine (24.4 mg, 0.24 mmol) in dichloromethane (6 ml) was added 2-methyl-5-nitrobenzene-1-sulfonyl chloride (53 mg, 0.18 mmol) at 0° C. The reaction was stirred at RT for 3 hours. The reaction mixture was poured into cold water and organic layer was separated. The aqueous layer was extracted with dichloromethane. The combined organic layer was dried over sodium sulfate and crude product was purified by column chromatography (silica gel, 2% acetone in chloroform) to obtain the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637670B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-583fdc6fb634442cb6aa1a8f5a4ddba2
출처 메모uspto-grants-2014_01