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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | N,N-bis(3-aminopropyl)methylamine | HCID 7777 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | toluene-4-sulfonic acid 7-oxo-7H-5,9-diaza-benzo[c]fluoren-6-yl ester | HCID 20829786 | — |
| 溶媒 | Dichloromethane | HCID 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-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06946472B2 |
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| 出典データセット | uspto-grants-2005_09 |
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| ORD ID | ord-47ebe698c6114793aab8c2c5be8b4eb9 |
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| 出典メモ | uspto-grants-2005_09 |
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