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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4215생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/4215

반응식

참여 물질

역할이름HCID투입량
반응물MAGNESIUM SILICATE (synthetic)HCID 61680—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물(2-Aminoethyl)(benzyl)methylamineHCID 3014812—
반응물N-(2-phenylsulfonylethyl)-2-propanamineHCID 13655034—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
생성물N-(1-Methylethyl)-N'-[2-[methyl(phenylmethyl)amino]ethyl]-N-[2-(phenylsulfonyl)ethyl]ureaHCID 20152874—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04724235
출처 데이터셋uspto-grants-1988_02
ORD IDord-082c10047ad64187a1aa3f32d4231702
출처 메모uspto-grants-1988_02