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HRID 334998Erstellt: 25. Oktober 2026

2-Chloro-4,6-dimethoxy-5-nitropyrimidine → HCID 57695130, Verbindung

https://huagongshe.com/reaction/334998

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-4,6-dimethoxy-5-nitropyrimidineHCID 10998537—
EduktHCID 178505764HCID 178505764—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 57695130HCID 5769513068,2%

Reaktionsschritte

(26) A solution of compound (25) (1.2 g, 5.5 mmol), 4-fluorobenzylzinc chloride (13.1 mL, 0.5 M in THF, 6.6 mmol), tetrakis(triphenylphosphine)palladium (0.13 g, 0.1 mmol) in THF (50 mL) was heated to refluxed for 3 hours under nitrogen. After it cooled to room temperature, the THF was removed in vacuo. The residue was diluted with ethyl acetate, washed with water and brine, dried over Na2SO4. After concentrated, the residue was purified by a column chromatography on silica gel eluting with 5% ethyl acetate in hexane to yield 2-(4-fluoro-benzyl)-4,6-dimethoxy-5-nitro-pyrimidine (26) (1.1 g, 63%). 1H NMR (CDCl3)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08883833B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-992b50dee6734a169c3ec7f10fa27b8c
Quellennotizuspto-grants-2014_11