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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N,N-bis(3-aminopropyl)methylamine | HCID 7777 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | toluene-4-sulfonic acid 7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-yl ester | HCID 20829786 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 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 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06946472B2 |
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| 출처 데이터셋 | uspto-grants-2005_09 |
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| ORD ID | ord-47ebe698c6114793aab8c2c5be8b4eb9 |
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| 출처 메모 | uspto-grants-2005_09 |
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