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HRID 496741作成日:2026年10月26日

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/reaction/496741

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-bis(3-aminopropyl)methylamineHCID 7777—
反応物Potassium CarbonateHCID 11430—
反応物toluene-4-sulfonic acid 7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-yl esterHCID 20829786—
溶媒DichloromethaneHCID 6344—
生成物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-oneHCID 10393889—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06946472B2
出典データセットuspto-grants-2005_09
ORD IDord-47ebe698c6114793aab8c2c5be8b4eb9
出典メモuspto-grants-2005_09