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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 745191생성일: 2026년 10월 24일

N,N-Diethylethylenediamine → N'-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N-[2-(phenylsulfinyl)ethyl]urea

https://huagongshe.com/ko/reaction/745191

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DiethylethylenediamineHCID 60993—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물N-[2-(phenylsulfinyl)ethyl]-2-propanamineHCID 13655080—
용매TetrahydrofuranHCID 8028—
생성물N'-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N-[2-(phenylsulfinyl)ethyl]ureaHCID 2015279555.9%

반응 단계

A mixture of 4.70 g (0.029 mole) of 1,1'-carbonyldiimidazole- and 3.07 g (0.0265 mole) of N,N-diethylethylenediamine in 400 ml of tetrahydrofuran was stirred at room temperature for 1 hr. A solution of 8.00 g (0.0245 mole) of N-[2-(phenylsulfinyl)ethyl]-2-propanamine in 50 ml of tetrahydrofuran was added, and the mixture was refluxed for 16 hr. The solvent was removed in vacuo, and the residue was dissolved in ether. The ether solution was extracted with several portions of water. The aqueous extract was extracted with ether and then with methylene chloride; these organic extracts were combined with the original ether solution. The organic solution was dried over magnesium sulfate, and the solvent was removed in vacuo to give an oil. Flash chromatography on silica gel (methanol) gave 4.84 g (55.9%) of oil: 1H NMR (CDC3), δ7.4-7.75 (m, 5, aromatic), 5.5) (br s, 1, NH) 4.12 (m, 1, (CH3)2CH), 2.8-3.7 (m, 6, SOCH2CH2 and NHCH2), 2.3-2.75 (m, 6, CH2N(CH2CH3)2), 0.8-1.3 (m, 12, CH3 groups).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04597902
출처 데이터셋uspto-grants-1986_07
ORD IDord-5438944b585246fd8fcd22c762032d19
출처 메모uspto-grants-1986_07