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HRID 324290Erstellt: 24. Oktober 2026

Ethyl Acetate → (+/-)-3-[(4-Bromo-2,6-dimethylphenyl)amino]-5-chloro-1-[1-(methoxymethyl)propyl]-2(1H)-pyrazinone

https://huagongshe.com/de/reaction/324290

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt4-Bromo-2,6-xylidineHCID 90549—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt3,5-dichloro-1-[1-(methoxymethyl)propyl]-2(1H)-pyrazinoneHCID 18452798—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(+/-)-3-[(4-Bromo-2,6-dimethylphenyl)amino]-5-chloro-1-[1-(methoxymethyl)propyl]-2(1H)-pyrazinoneHCID 1548577384,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To (+/−)-3,5-dichloro-1-[1-(methoxymethyl)propyl]-2(1H)-pyrazinone (300 mg) and 4-bromo-2,6-dimethylaniline (238 mg) in THF (anhydrous, 9.4 mL) at 0° C. was added sodium bis(trimethylsilyl)amide (1.0 M/THF, 2.6 mL). The mixture was stirred at 0° C. for 10 minutes. Ethyl acetate (100 mL) was added and washed with water (25 mL) and brine (25 mL). The organic layer was dried over MgSO4 and concentrated and the crude product was chromatographed on silica gel using ethyl acetate/hexane (1:4) as eluent. The product was then crystallized from ethyl acetate/hexane to afford the title compound (419 mg). Elemental analysis calcd. for C17H21N3O2BrCl: C, 49.23; H, 5.10; N, 10.13. Found: C, 49.33; H, 5.05; N, 10.09.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218391B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-969329ba337f44918f532a4b56db4fc7
Quellennotizuspto-grants-2001_04