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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606034생성일: 2026년 10월 26일

Triethylamine → 4-chloro-2-(ethoxymethyl)-1-[(3-methyl-4,5-dihydroisoxazol-5-yl)methyl]-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/606034

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethanimidoyl chloride, N-hydroxy-HCID 69633—
반응물1-allyl-4-chloro-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolineHCID 86091452—
용매DichloromethaneHCID 6344—
생성물4-chloro-2-(ethoxymethyl)-1-[(3-methyl-4,5-dihydroisoxazol-5-yl)methyl]-1H-imidazo[4,5-c]quinolineHCID 8661687075.1%

반응 단계

Triethylamine (1.04 mL, 7.46 mmol) was added to a 0° C. solution of 1-allyl-4-chloro-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinoline (1.50 g, 4.97 mmol) and N-hydroxyethanimidoyl chloride (581 mg, 6.21 mmol) in dichloromethane (80 mL). The reaction solution was allowed to warm slowly to room temperature and stir overnight under a nitrogen atmosphere. After 20 hours, the solution was washed with saturated aqueous sodium bicarbonate and brine, dried over magnesium sulfate, filtered, and concentrated. The crude product was purified by flash chromatography (silica gel, elution with 98:2 dichloromethane/methanol) to yield 4-chloro-2-(ethoxymethyl)-1-[(3-methyl-4,5-dihydroisoxazol-5-yl)methyl]-1H-imidazo[4,5-c]quinoline (1.34 g) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915281B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-fb28a50943984e76b1da50232fa71d68
출처 메모uspto-grants-2011_03