Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1836196Erstellt: 26. Oktober 2026

Sodium hydride → 6-Amino-2-methoxy-4-(4-acetoxybutyl)pyrimidine

https://huagongshe.com/reaction/1836196

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt1-Butanol, 4-bromo-, 1-acetateHCID 78491—
EduktLithium BromideHCID 82050—
Edukt6-Amino-2-methoxy-3,4-dihydropyrimidin-4-oneHCID 135404214—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-Amino-2-methoxy-4-(4-acetoxybutyl)pyrimidineHCID 2349908816%

Reaktionsschritte

Sodium hydride (60% dispersion in mineral oil, 8.2 g, 205 mmol) was added to a mixture of 6-amino-2-methoxy-4-pyrimidone (24.0 g, 170 mmol) in DMF at 0° C. After 0.5 hours, lithium bromide (19.2 g, 221 mmol) was added to the mixture and stirred for 0.5 hours at room temperature. The temperature was slowly increased to 70° C., and a solution of 4-bromobutyl acetate (50 g, 256 mmol) in DMF was added dropwise to the reaction mixture. The mixture was stirred at 70° C. for 3 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was purified by chromatography on silica gel using CHCl3/MeOH (1-5%) as eluent to give first 6.5 g (15%) of 6-amino-2-methoxy-4-(4-acetoxybutyl)pyrimidine as a white solid followed by 23.4 g (yield 54%) of 6-amino-2-methoxy-3-(4-acetoxybutyl)-4-pyrimidone as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06777420B2
Quelldatensatzuspto-grants-2004_08
ORD IDord-f59ba468b9db4e56939ac0bf61cb8952
Quellennotizuspto-grants-2004_08