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HRID 445537Erstellt: 24. Oktober 2026

Diphosgene → 8-bromo-1-(1,3-dimethyl-1H-pyrazol-4-yl)-1,3-dihydro-imidazo[4,5-c]quinolin-2-one

https://huagongshe.com/de/reaction/445537

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiphosgeneHCID 10426—
Edukt6-bromo-4-N-(1,3-dimethylpyrazol-4-yl)quinoline-3,4-diamineHCID 59619708—
LösungsmittelDichloromethaneHCID 6344—
Produkt8-bromo-1-(1,3-dimethyl-1H-pyrazol-4-yl)-1,3-dihydro-imidazo[4,5-c]quinolin-2-oneHCID 59619891—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 6-bromo-N*4*-(1,3-dimethyl-1H-pyrazol-4-yl)-quinoline-3,4-diamine (Stage A.2, 3.15 g, 8.15 mmol) and TEA (1.36 ml, 9.79 mmol) in DCM (65 ml) was added under argon, after cooling with an ice-bath, a solution of trichloromethyl chloroformate (1.08 ml, 8.97 mmol in DCM (65 ml). The mixture was stirred for 25 min at 0° C. Then the RM was quenched with sat. aqueous NaHCO3 (300 ml) and 10 M aqueous NaOH (4 ml) and well stirred. The phases were separated and extracted with EtOAc (3×). The combined organic layers were washed with brine (2×), dried over Na2SO4, filtered and evaporated to dryness to give the title compound as a brownish solid (HPLC tR 2.29 min (Method A); M+H=360; M−H=358 MS-ES)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476294B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-246aaacf031e4a2598929e88d677f106
Quellennotizuspto-grants-2013_07