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HRID 745191作成日:2026年10月26日

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

https://huagongshe.com/reaction/745191

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DiethylethylenediamineHCID 60993—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物N-[2-(phenylsulfinyl)ethyl]-2-propanamineHCID 13655080—
溶媒TetrahydrofuranHCID 8028—
生成物N'-[2-(Diethylamino)ethyl]-N-(1-methylethyl)-N-[2-(phenylsulfinyl)ethyl]ureaHCID 2015279555.9%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04597902
出典データセットuspto-grants-1986_07
ORD IDord-5438944b585246fd8fcd22c762032d19
出典メモuspto-grants-1986_07