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HRID 1371309作成日:2026年10月26日

Propyl Isothiocyanate → N-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N'-propylthiourea

https://huagongshe.com/reaction/1371309

反応式

関与物質

役割名称HCID仕込み量
反応物Propyl IsothiocyanateHCID 69403—
反応物1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amineHCID 12148992—
溶媒PyridineHCID 1049—
溶媒ChloroformHCID 6212—
生成物N-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N'-propylthioureaHCID 99545256.6%

反応手順

A solution of propyl isothiocyanate (0.78 g, 7.72 mmol) in chloroform (5 mL) was added at ambient temperature to a solution of 1-(4-aminobutyl)-2-phenyl-1H-imidazo[4,5-c]quinolin-4-amine (0.256 g, 7.72 mmol) in a mixture of chloroform (25 mL) and pyridine (5 mL). The reaction mixture was maintained at ambient temperature over the weekend. The reaction was quenched with ethanol and then concentrated under vacuum to provide a pale orange syrup. This material was purified by flash chromatography (silica gel, eluting with 10% methanol in dichloromethane). The pure fractions were combined and concentrated under vacuum to provide 0.22 g of N-[4-(4-amino-2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-N′-propylthiourea as a white solid, m.p. 113–116° C. Mass spec M+1=433.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07157453B2
出典データセットuspto-grants-2007_01
ORD IDord-9c77339e09194ecba97e92c4317ed771
出典メモuspto-grants-2007_01