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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270700Erstellt: 25. Oktober 2026

Methyl iodide → 2(1h)-Quinolinone,3-(2,6-dichloro-3-nitrophenyl)-1-methyl-

https://huagongshe.com/reaction/270700

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt3-(2,6-dichloro-3-nitro-phenyl)-1H-quinolin-2-oneHCID 59833933—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2(1h)-Quinolinone,3-(2,6-dichloro-3-nitrophenyl)-1-methyl-HCID 5983380835,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 3-(2,6-dichloro-3-nitro-phenyl)-1H-quinolin-2-one (0.21 g, 0.6266 mmol) in DMF (5.0 mL) is added HNa (30.1 mg, 60%, 0.752 mmol) and IMe (120.1 mg, 0.846 mmol) at 0° C. After the mixture is stirred for two hours at 0° C., the mixture is diluted with EtOAc and washed with saturated K2CO3, brine and water. The organic layer is dried, filtered and concentrated to give crude product, which is purified by flash silica gel column, eluting with CH2Cl2 (100%) gradient to CH2Cl2/MeOH (2N NH3) (95/5), t give the titled intermediate as a solid (78 mg, 35.8%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07449582B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-60dd77d7c65f4499bcef4f71040252c5
Quellennotizuspto-grants-2008_11