돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4214생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/4214

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—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
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 chloroformdiethyl 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 oganic 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 번호US04724235
출처 데이터셋uspto-grants-1988_02
ORD IDord-bfa7dcd3f23744c99a5e0a575455a555
출처 메모uspto-grants-1988_02