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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1154743Erstellt: 26. Oktober 2026

1-Bromopropane → Itraconazole Impurity 8

https://huagongshe.com/reaction/1154743

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-BromopropaneHCID 7840—
EduktSodium hydrideHCID 24758—
Edukt2,4-Dihydro-4-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)-3H-1,2,4-triazol-3-oneHCID 4246597—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktItraconazole Impurity 8HCID 1336824865%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

10 Parts of 2,4-dihydro-4-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}-3H-1,2,4-triazol-3-one are dissolved in 300 parts of dimethyl sulfoxide at 100° C. Then there are added 1.6 parts of sodium hydride dispersion 50% and stirring is continued while the mixture is allowed to cool to about 50° C. 3.9 Parts of 1-bromopropane are added and the whole is stirred overnight at room temperature. The reaction mixture is poured onto water and the product is extracted with trichloromethane. The extract is washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is triturated in 2-propanol. The product is filtered off and dried; yielding 7.5 parts (65%) of 2,4-dihydro-4-{4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl}-2-propyl-3H-1,2,4 -triazol-3-one.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04490530
Quelldatensatzuspto-grants-1984_12
ORD IDord-3892382c06fd4adea71bfc5a35e96fe7
Quellennotizuspto-grants-1984_12