HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1795910Erstellt: 26. Oktober 2026
Dichloromethane → N1-[4-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-5-(dimethylamino)-1-naphthalenesulfonamide
https://huagongshe.com/reaction/1795910
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Dansyl chloride | HCID 11801 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 1-(4-Aminobutyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amine | HCID 15538226 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N1-[4-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-5-(dimethylamino)-1-naphthalenesulfonamide | HCID 15538227 | 71,5% |
Reaktionsschritte
5-Dimethylamino-1-naphthalenesulfonyl chloride (1.82 g, 6.74 mmol) was added to a mixture of N,N-diisopropylethylamine (1.23 mL, 7.06 mmol), dichloromethane (15 mL) and 1-(4-aminobutyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amine (2.0 g, 6.42 mmol). The reaction mixture was allowed to stir at ambient temperature overnight. Methanol was added to the reaction mixture until a clear solution was obtained. Silica gel was added to the reaction mixture and then the solvents were removed. The silica gel was placed in a column and then eluted with chloroform in a stepwise gradient to 9:1 chloroform:methanol. The resulting product was recrystallized from N,N-dimethylformamide and deionized water to provide 2.5 g of N1-[4-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-5-(dimethylamino)-1-naphthalenesulfonamide as a yellow crystalline solid, m.p. 223–224° C. Analysis: Calculated for C30H36N6O2S: %C, 66.15; %H, 6.66; %N, 15.43; Found: %C, 66.36; %H, 6.34; %N, 15.23.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07030131B2 |
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| Quelldatensatz | uspto-grants-2006_04 |
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| ORD ID | ord-894073caa2c34fb7924afb861edc40c9 |
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| Quellennotiz | uspto-grants-2006_04 |
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