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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 745182생성일: 2026년 10월 26일

1,1'-Carbonyldiimidazole → N-(1-Methylethyl)-N'-[2-[methyl-(2-phenylethyl)amino]ethyl]-N-[2-(phenylsulfonyl)ethyl]urea hemihydrate

https://huagongshe.com/reaction/745182

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물N-Methyl-N-(2-phenylethyl)ethane-1,2-diamineHCID 12488261—
반응물N-(2-phenylsulfonylethyl)-2-propanamineHCID 13655034—
반응물Ethylacetate acetoneHCID 21584569—
용매TetrahydrofuranHCID 8028—
용매Chloroform etherHCID 21911965—
생성물N-(1-Methylethyl)-N'-[2-[methyl-(2-phenylethyl)amino]ethyl]-N-[2-(phenylsulfonyl)ethyl]urea hemihydrateHCID 70419535—

반응 단계

A solution of 1,1'-carbonyldiimidazole (8.12 g, 0.05 mole) and N-methyl-N-(2-phenylethyl)-1,2-ethanediamine, 8.0 g (0.0045 mole) in 300 ml of tetrahydrofuran was stirred for 2 hours at room temperature. To the mixture was added 9.37 g (0.0412 mole) of 1-methyl-N-[2-(phenylsulfonyl)ethyl]ethanamine and the reaction was heated at gentle reflux overnight. The reaction was stripped to dryness and dissolved in chloroform-diethyl ether (50-50 v/v) and extracted with water. The organic phase was extracted with 1N sulfuric acid. (Approximately half the product was extracted with acid and half remained in the organic layer). The organic layer was extracted with dilute sodium hydroxide, dried, filtered, and the solvent removed to give an oil. The oil was subjected to column chromatography on Silica Gel using acetone-ethyl acetate as a eluant. This furnished 0.5 g (2.8%) of oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04597902
출처 데이터셋uspto-grants-1986_07
ORD IDord-0ae0a9dc6c934b61a16309de49d0b18f
출처 메모uspto-grants-1986_07