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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2404993생성일: 2026년 10월 25일

Dimethyl Sulfoxide → 4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butanal

https://huagongshe.com/reaction/2404993

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butan-1-olHCID 68996527—
용매DichloromethaneHCID 6344—
생성물4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butanalHCID 86626643100.1%

반응 단계

Under a nitrogen atmosphere, dimethylsulfoxide (3.6 mL, 1.5 eq.) and oxalyl chloride (3.5 mL, 1.1 eq.) were sequentially added dropwise to chilled (dry ice/acetone bath) dichloromethane (100 mL). A solution of 4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butan-1-ol (10 g, 37 mmol, 1 eq.) in dichloromethane was added dropwise. Triethylamine (15.5 mL, 3 eq.) was added. The ice bath was removed and the reaction mixture was allowed to warm to ambient temperature. After about 2 hours analysis by TLC indicated that the reaction was complete. The reaction mixture was diluted with dichloromethane (175 mL) and water (200 mL) and made basic (pH 10) with aqueous 5% sodium carbonate. The organic layer was washed sequentially with water (2×200 mL) and brine (150 mL) and then concentrated under reduced pressure to provide 9.9 g of 4-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butanal.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08802853B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-a7310def4c1848dea55c9d98d05de177
출처 메모uspto-grants-2014_08