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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7626Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-[7-(3-Fluoro-benzyloxy)-4-oxo-4H-quinazolin-3-yl]-acetamide

https://huagongshe.com/de/reaction/7626

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt3-Fluorobenzylic alcoholHCID 68008—
EduktSodiumHCID 5360545—
Edukt7-Fluoroquinazolin-4(3H)-oneHCID 135398496—
Edukt7-(3-Fluoro-benzyloxy)-3H-quinazolin-4-oneHCID 135752716—
LösungsmittelWaterHCID 962—
Produkt2-[7-(3-Fluoro-benzyloxy)-4-oxo-4H-quinazolin-3-yl]-acetamideHCID 986218061%

Reaktionsschritte

7-(3-Fluoro-benzyloxy)-3H-quinazolin-4-one: Sodium (1.8 g, 78.6 mmol) was added portionwise to 3-fluorobenzyl alcohol and the resulting mixture heated at 80–90° C. for 4 h under Argon. The resulting suspension was cooled to rt and 7-fluoro-3H-quinazolin-4-one (3.2 g, 19.5 mmol) was added and the resulting mixture heated at 130–140° C. for 14 h. The solid formed was then dissolved with water (400 mL) and the mixture acidified to pH 3–4 with HCl (4 N). The resulting precipitate was then filtered off, washed with water (100 mL) and diethylether (100 mL). Recrystallisation from tetrahydrofuran: ethylacetate (1:1) afforded the title compound (3.2 g, 61%) as white crystals. MS: m/e=271.3 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087612B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-af083bdcb1c9493f8949656570ce9951
Quellennotizuspto-grants-2006_08