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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 487361Erstellt: 23. Oktober 2026

Bicyclo(2.2.1)heptan-2-one → 1-Methyl-5-[3-(Bicyclo[2.2.1]hept-2-ylamino)-4-Methoxyphenyl]-2-Imidazolidinone

https://huagongshe.com/de/reaction/487361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBicyclo(2.2.1)heptan-2-oneHCID 10345—
EduktSodium HydroxideHCID 14798—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt1-Methyl-5-(3-Amino-4-Methoxyphenyl)-2-ImidazolidinoneHCID 19378882—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-Methyl-5-[3-(Bicyclo[2.2.1]hept-2-ylamino)-4-Methoxyphenyl]-2-ImidazolidinoneHCID 1401020510,1%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

The aniline of Example 51 (3.07 g, 17.95 mmol) is dissolved in 60 ml of glacial acetic acid and to this is added norcamphor (2.37 g, 21.54 mmol). The reaction is cooled to 5° C. and to it is added sodium cyanoborohydride (1.36 g, 21.54 mmol). The reaction is poured onto ice and is pH adjusted to 7 with 1 normal NaOH solution. The aqueous is extracted with methylene chloride dried over MgSO4, filtered and concentrated in vacuo to afford a brown oil which is flashed on SiO2 with ethyl acetate as the eluent. The appropriate fractions are combined and concentrated in vacuo to yield a white paste which is tritarted with ether to yield 0.57 g (10%) of the product as a white crystalline solid. MP=171°-174° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05294730
Quelldatensatzuspto-grants-1994_03
ORD IDord-677753999e4f43728c5026a3dab1ba62
Quellennotizuspto-grants-1994_03