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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430062생성일: 2026년 10월 25일

Putrescine → 2-(4-Aminobut-1-ylamino)-4-methoxyquinoline

https://huagongshe.com/reaction/430062

반응식

참여 물질

역할이름HCID투입량
반응물PutrescineHCID 1045—
반응물2-Chloro-4-methoxyquinolineHCID 12369166—
용매DichloromethaneHCID 6344—
생성물2-(4-Aminobut-1-ylamino)-4-methoxyquinolineHCID 1835370647%

반응 단계

2-Chloro-4-methoxyquinoline (prepared as for 2-chloro-4-ethoxyquinoline but using methanol as solvent; 3.873 g, 20 mmol) and 1,4-diaminobutane (12.3 g, 140 mmol) were heated at 60° C. for 50 h. The solution was then reduced in volume in vacuo, and diluted with dichloromethane. The solid was filtered off and washed with dichloromethane. The filtrate was evaporated to dryness and purified by flash chromatography, eluting with 0-10% ‘10% ammonia in methanol’ in dichloromethane, to give 2-(4-aminobut-1-ylamino)-4-methoxyquinoline as a white solid (2.29 g, 47%). This material (2.142 g, 8.73 mmol) in concentrated hydrochloric acid (80 ml) was gently refluxed for 15 h, and then evaporated to dryness to give the title compound as a white foam (2.65 g, 99%); δH (CD3OD) 1.8-1.9 (4H, m), 2.95-3.05 (2H, m), 3.5-3.6 (2H, m), 6.36 (1H, s), 7.46 (1H, t), 7.7-7.9 (2H, m), 8.45(1H, d): MS (ES+) 232 (100%, MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06320051B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-918e11715e534a4cb6a78f499bb40b68
출처 메모uspto-grants-2001_11