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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4230생성일: 2026년 10월 24일

Methanol → N'-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N-[5-(phenylsulfonyl)pentyl]urea hydrate

https://huagongshe.com/ko/reaction/4230

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물N,N-DiethylethylenediamineHCID 60993—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물N-(1-methylethyl)-5-(phenylsulfonyl)-1-pentanamineHCID 13655070—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
생성물N'-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N-[5-(phenylsulfonyl)pentyl]urea hydrateHCID 2015283766.6%

반응 단계

A solution of 1,1'-carbonyldiimidazole (4.54 g, 0.028 mole) and N,N-diethylethylenediamine (2.90 g, 0.025 mole) in tetrahydrofuran was stirred for 1 hr at room temperature. A solution of N-(1-methylethyl)-5-(phenylsulfonyl)-1-pentanamine (6.74 g, 0.025 mole) in tetrahydrofuran (dried over 4 A molecular sieves) was added and the resulting solution was heated over night at gentle reflux. The reaction mixture was stripped to dryness and the residue dissolved in chloroform. The chloroform layer was extracted with water, dried (anhydrous sodium sulfate), filtered and the solvent removed to give a brown oil. The brown oil was subjected to flash column chromatography on Silica Gel using methanol for elution. Fractions of similar purity were combined, solvent removed, and the oil dried in vacuo at 60° C. overnight. This produced 7.00 g (66.6% yield) of brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04724235
출처 데이터셋uspto-grants-1988_02
ORD IDord-3bf903c0996240489547e5913b65a55e
출처 메모uspto-grants-1988_02