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HRID 4225作成日:2026年10月25日

1,1'-Carbonyldiimidazole → N-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N'-[2-(phenylsulfonyl)ethyl]urea

https://huagongshe.com/reaction/4225

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物2-(Benzenesulfonyl)ethan-1-amineHCID 3545497—
反応物Diethyl((2-((propan-2-yl)amino)ethyl))amineHCID 12639037—
溶媒TetrahydrofuranHCID 8028—
生成物N-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N'-[2-(phenylsulfonyl)ethyl]ureaHCID 20152862—

反応手順

A mixture of 6.96 g (0.0376 mole) of 2-phenylsulfonylethanamine and 6.64 g (0.041 mole) of 1,1'-carbonyldiimidazole in 400 ml of tetrahydrofuran was stirred at room temperature for 1 hr. A solution of 6.16 g (0.039 mole) of N-[2-(diethylamino)ethyl]-2-propanamine in 50 ml of tetrahydrofuran was added, and the mixture was refluxed for 13 hr. The solvent was removed in vacuo, and the residue was dissolved in a 50/50 mixture of ether and methylene chloride. The solution was extracted with water and was dried over magnesium sulfate. The solvent was removed in vacuo in give an oil. Flash chromatography on silica gel (methanol) gave 5.74 g (41.36%) of clear, colorless oil:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04724235
出典データセットuspto-grants-1988_02
ORD IDord-55f9bf21ef824a7cb9d80cb03f44809d
出典メモuspto-grants-1988_02