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HRID 373731作成日:2026年10月27日

Methanol → 1-(Ethoxycarbonylaminocarbonyl)-2-(3,5-dimethoxy-4-hydroxyphenyl)-4,5-bis(4-diethylaminophenyl)imidazole

https://huagongshe.com/reaction/373731

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物ethyl N-carbonylcarbamateHCID 300166—
反応物2-(3,5-Dimethoxy-4-hydroxyphenyl)-4,5-bis(4-diethylaminophenyl)imidazoleHCID 136006555—
溶媒ChloroformHCID 6212—
生成物1-(Ethoxycarbonylaminocarbonyl)-2-(3,5-dimethoxy-4-hydroxyphenyl)-4,5-bis(4-diethylaminophenyl)imidazoleHCID 13603275761.3%

反応手順

In 20 ml of chloroform, 0.8 g of 2-(3,5-dimethoxy-4-hydroxyphenyl)-4,5-bis(4-diethylaminophenyl)imidazole obtained in Example 1 (2) was dissolved. Then, 0.7 g of ethoxycarbonyl isocyanate (mfd. by Aldrich Chemical Co. Inc.) was added to the resulting solution and the reaction was carried out at room temperature for 5 hours with stirring. After the reaction, 5 ml of methanol was added to the reaction solution to decompose excess ethoxycarbonyl isocyanate, followed by removal of the solvent by distillation under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent: a mixed solvent of ethyl acetate and n-hexane) to give 0.6 g of green crystals of 1-(ethoxycarbonylaminocarbonyl)-2-(3,5-dimethoxy-4-hydroxyphenyl)-4,5-bis(4-diethylaminophenyl)imidazol having a m.p. of 60° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05164512
出典データセットuspto-grants-1992_11
ORD IDord-64a58222fb414e52912b0cce693b31ca
出典メモuspto-grants-1992_11