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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 496741생성일: 2026년 10월 24일

N,N-bis(3-aminopropyl)methylamine → 6-(3-{methyl-[3-(7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-ylamino)-propyl]-amino}-propylamino)-5,9-diaza-benzo[c]fluoren-7-one

https://huagongshe.com/ko/reaction/496741

반응식

참여 물질

역할이름HCID투입량
반응물N,N-bis(3-aminopropyl)methylamineHCID 7777—
반응물Potassium CarbonateHCID 11430—
반응물toluene-4-sulfonic acid 7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-yl esterHCID 20829786—
용매DichloromethaneHCID 6344—
생성물6-(3-{methyl-[3-(7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-ylamino)-propyl]-amino}-propylamino)-5,9-diaza-benzo[c]fluoren-7-oneHCID 10393889—

반응 단계

A mixture of toluene-4-sulfonic acid 7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-yl ester (Reference Example 6c-2) (90 mg) and N1-(3-amino-propyl)-N1-methyl-propane-1,3-diamine (WAKO PURE CHEMICAL: 15 mg) and potassium carbonate (37 mg) was suspended in dichloromethane (10 ml) and heated at reflux temperature for five days under nitrogen. The mixture was roughly purified by short silica gel column chromatography developed by dichloromethane-methanol=100:1 and dichloromethane-methanol=1:1. The fractions that contained the desired product were combined and evaporated to dryness and purified again by silica gel thin layer chromatography developed by dichloromethane-methanol-ammonia water=90:10:1. The desired compound was obtained as a dark reddish powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06946472B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-47ebe698c6114793aab8c2c5be8b4eb9
출처 메모uspto-grants-2005_09