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HRID 4215作成日:2026年10月26日

MAGNESIUM SILICATE (synthetic) → N-(1-Methylethyl)-N'-[2-[methyl(phenylmethyl)amino]ethyl]-N-[2-(phenylsulfonyl)ethyl]urea

https://huagongshe.com/reaction/4215

反応式

関与物質

役割名称HCID仕込み量
反応物MAGNESIUM SILICATE (synthetic)HCID 61680—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物(2-Aminoethyl)(benzyl)methylamineHCID 3014812—
反応物N-(2-phenylsulfonylethyl)-2-propanamineHCID 13655034—
溶媒ChloroformHCID 6212—
溶媒TetrahydrofuranHCID 8028—
生成物N-(1-Methylethyl)-N'-[2-[methyl(phenylmethyl)amino]ethyl]-N-[2-(phenylsulfonyl)ethyl]ureaHCID 20152874—

反応手順

A solution of 17.90 g (0.045 mole) of N-methyl-N-(phenylmethyl)-1,2-ethanediamine and 1,1'-carbonyldiimidazole (0.05 mole) in 100 ml of tetrahydrofuran was stirred at room temperature for 1 hour. To the mixture was added 10.52 g, (0.04 mole) of 1-methyl-N-[2-(phenysulfonyl)ethyl]ethanamine and the resulting solution heated overnight at gentle reflux. The reaction mixture was stripped to dryness and partitioned between chloroform and water; removal of chloroform gave a dark brown oil. The oil was dissolved in chloroform and extracted with 1N sulfuric acid (saturated with sodium chloride). The acidic layer was made alkaline, extracted with chloroform, and the solvent removed to give a light brown oil. The oil was subjected to chromatography on a Florisil column and eluted with methanol-methylene chloride. After combining appropriate fractions from the column and removing solvent, an oil was obtained. The oil was triturated with diethyl ether and dried at 80° C. in vacuo overnight. This furnished 6.75 g (40.4%) of clear 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-082c10047ad64187a1aa3f32d4231702
出典メモuspto-grants-1988_02