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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 745189Erstellt: 26. Oktober 2026

1,1'-Carbonyldiimidazole → N'-[2-(Diethylamino)-1-methylethyl]-N-(1-methylethyl)-N-[2-(phenylsulfonyl)ethyl]urea

https://huagongshe.com/reaction/745189

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktN-(2-phenylsulfonylethyl)-2-propanamineHCID 13655034—
Edukt(2-Aminopropyl)diethylamineHCID 16643481—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN'-[2-(Diethylamino)-1-methylethyl]-N-(1-methylethyl)-N-[2-(phenylsulfonyl)ethyl]ureaHCID 2015278959,5%

Reaktionsschritte

A mixture of 12.15 g (0.075 mole) of 1,1'-carbonyl diimidazole and 7.50 g (0.0476 mole) of 1-diethylamino-2-propanamine in 400 ml of tetrahydrofuran was stirred at room temperature for 1 hr. A solution of 12.26 g (0.054 mole) of N-[2-(phenylsulfonyl)ethyl]-2-propanamine in 50 ml of tetrahydrofuran was added, and the solution was refluxed for 19 hr. The solvent was removed in vacuo, and the residue was dissolved in a 50/50 mixture of methylene chloride and ether. The organic solution was extracted with several portions of water and was dried over magnesium sulfate. The solvent was removed in vacuo to give an oil. Flash chromatography on silica gel (elution with methanol) gave 10.87 g (52.3 g) of clear colorless oil. 1H NMR (CDCl3)δ7.5-8.15 (m, s. aromatic), 5.35 (br s, 1, NH), 4.1 (m, 1, (CH3)2CH), 3.45-4.0 (m, 1. NHCH(CH3)CH2), 2.5-2.85 (m, 6, CH2CH3)), 0.85-1.3 (m, 15, CH3 groups).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04597902
Quelldatensatzuspto-grants-1986_07
ORD IDord-d6f7b9cd8a144e3088b7dc53097cca2d
Quellennotizuspto-grants-1986_07