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HRID 2180263作成日:2026年10月25日

Dichloromethane → N1-[4-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-5-(dimethylamino)-1-naphthalenesulfonamide

https://huagongshe.com/reaction/2180263

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Dansyl chlorideHCID 11801—
反応物DiisopropylethylamineHCID 81531—
反応物1-(4-Aminobutyl)-2-butyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 15538226—
溶媒MethanolHCID 887—
生成物N1-[4-(4-amino-2-butyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-5-(dimethylamino)-1-naphthalenesulfonamideHCID 1553822771.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06888000B2
出典データセットuspto-grants-2005_05
ORD IDord-171d261987204481b9e5bc90dcd1e305
出典メモuspto-grants-2005_05