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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 983452Erstellt: 24. Oktober 2026

Water → (+/-)-[3-[bis(phenylmethyl)amino]-2-hydroxypropyl]-2(1H)pyrimidinone

https://huagongshe.com/de/reaction/983452

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
EduktN,N-dibenzyl-1-(oxiran-2-yl)methanamineHCID 11276836—
EduktHCID 178479648HCID 178479648—
LösungsmittelMethanolHCID 887—
LösungsmittelTolueneHCID 1140—
Produkt(+/-)-[3-[bis(phenylmethyl)amino]-2-hydroxypropyl]-2(1H)pyrimidinoneHCID 2256081845%

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

A solution of 2-hydroxypyrimidine hydrochloride (1:1) (0.075 mol) in methanol (150 ml) was stirred for 30 minutes and then added to a solution of sodium carbonate (0.075 mol) in methanol (20 ml). The mixture was stirred and refluxed for 15 minutes, and cooled to 55° C. A solution of N,N-bis(phenylmethyl)oxiranmethanamine (0.075 mol) in toluene (160 ml) was added dropwise and the reaction mixture was stirred at 50° C. overnight. Water (75 ml) was added and the mixture was stirred at 55° C. for 15 minutes. The organic layer was separated, washed with water, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH3OH/CH2Cl2 97/3). The pure fractions were collected and the solvent was evaporated, yielding 11.8 g (45%) of (±)-1-[3-[bis(phenylmethyl)amino]-2-hydroxypropyl]-2(1H)pyrimidinone (interm. 2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06864273B1
Quelldatensatzuspto-grants-2005_03
ORD IDord-9eb688e745404af191d496479c6c7af9
Quellennotizuspto-grants-2005_03