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HRID 16318Erstellt: 25. Oktober 2026

2,6-Difluorobenzoyl chloride → 2-(3,4,5-Trimethoxyphenylamino)-6-[4-(2,6-difluorophenylcarbonyl)-amino phenyl]-pyrazine

https://huagongshe.com/reaction/16318

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,6-Difluorobenzoyl chlorideHCID 87438—
Edukt2-(3,4,5-Trimethoxyphenylamino)-6-(4-aminophenyloxy)-pyrazineHCID 59343439—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(3,4,5-Trimethoxyphenylamino)-6-[4-(2,6-difluorophenylcarbonyl)-amino phenyl]-pyrazineHCID 6691256630%

Reaktionsschritte

Using Method LL with 2-(3,4,5-trimethoxyphenylamino)-6-(4-aminophenyloxy)-pyrazine (50 mg, 0.14 mmol) and 2,6-difluoro-phenylcarbonyl chloride (30 mg, 0.17 mmol), and purification by column chromatography (AcOEt), the title compound was obtained (21 mg). Yield: 30%. 1H NMR (250 MHz, DMSO-d6) δ 3.65 (s, 3H, [CH3O]4), 3.85 (s, 6H, [CH3O]3+5), 7.27 (s, 2H, Harom2′+6′), 7.45-7.47 (m, 1H, Harom 3″), 7.79-7.84 (m, 2H, Harom 4″+5″), 7.86 (d, 2H, Harom 3+5, J=8.3 Hz), 8.14 (s, 1H, HPz 5), 8.15 (d, 2H, Harom 2+6, J=6.7 Hz), 8.52 (s, 1H, HPz 3), 9.56 (s, 1H, NH), 10.61 (s, 1H, NHamide). m/z 493.2 [(M+H)+ calcd for C26H22F2N4O6 492.2].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737152B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-41b43b43a566470582a78c52bf67495b
Quellennotizuspto-grants-2010_06