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HRID 231313Erstellt: 23. Oktober 2026

Sodium Bicarbonate → 2-[4-(1,2,3,4-Tetrahydro-8-hydroxy-2-naphthalenyl)-1-piperazinyl]pyrimidine

https://huagongshe.com/de/reaction/231313

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
EduktBoronHCID 5462311—
Edukt2-(4-(1,2,3,4-Tetrahydro-8-methoxy-2-naphthalenyl)-1-piperazinyl]-pyrimidine hydrochlorideHCID 14479999—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-[4-(1,2,3,4-Tetrahydro-8-hydroxy-2-naphthalenyl)-1-piperazinyl]pyrimidineHCID 1448000270,9%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

2-(4-(1,2,3,4-Tetrahydro-8-methoxy-2-naphthalenyl)-1-piperazinyl]-pyrimidine hydrochloride (1.62 g, 5.0 mmole) was dissolved in 185 ml of methylene chloride and cooled to -78° C. in a dry ice/acetone bath. A mixture of 15 ml of 1 M boron triboromide and 15 ml of methylene chloride was added. The reaction mixture was allowed to come to room temperature and it was then stirred for three days. The reaction was then poured into a saturated NaHCO3 solution and the product extracted with 600 ml of chloroform. This solution was dried over MgSO4, filtered, and concentrated in vacuum. The residue was column chromatographed on 100 g of silica gel with 5% methanol/chloroform and the crude title compound thus obtained was crystallized from isopropanol with addition of 4 N isopropanolic HCl and recrystallized from acetone to give 1.1 g of the title compound as the hydrochloride, monohydrate, m.p.>300° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04845221
Quelldatensatzuspto-grants-1989_07
ORD IDord-9d94aa52a6f94522be50fbb6f5df93e1
Quellennotizuspto-grants-1989_07