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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1164985Erstellt: 25. Oktober 2026

Triethylamine → Methyl 2-[2-Hydroxy-3-[N-[2-[N-(phenylaminocarbonyl)amino]ethyl]amino]propoxy]benzoate

https://huagongshe.com/reaction/1164985

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethyl 2-(oxiran-2-ylmethoxy)benzoateHCID 279510—
Edukt3-(2-Aminoethyl)-1-phenylurea hydrochlorideHCID 19863750—
LösungsmittelMethanolHCID 887—
ProduktMethyl 2-[2-Hydroxy-3-[N-[2-[N-(phenylaminocarbonyl)amino]ethyl]amino]propoxy]benzoateHCID 130309447,5%

Reaktionsschritte

4.8 g of N-phenyl-N'-(2-aminoethyl)urea HCl salt (0.024 mole) was placed in 100 ml of methanol, and 2.5 g of triethylamine (0.024 mole) was added. While this reaction mixture was being stirred, a solution of 5 g of methyl 2-(2,3-epoxypropoxy)benzoate (0.024 mole) in 25 ml methanol was added slowly. The solution was then heated to reflux for 4 hours. The methanol was removed under reduced pressure and the resulting gel-like solid was dissolved in 100 ml of methylene chloride. The organic layer was washed twice with 100 ml of water and dried over anhydrous magnesium sulfate. Removal of the methylene chloride left an oil which was dissolved in 50 ml of methanol/ethyl ether (1:1) from which the product crystallized slowly upon refrigeration to afford 0.7 g (7.5%) of product having a melting point of 133°-134° C. The compound was identified by its NMR spectrum and elemental analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04906661
Quelldatensatzuspto-grants-1990_03
ORD IDord-c10f3505907744b89d2b71a5cc55d86d
Quellennotizuspto-grants-1990_03