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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174891Generated: October 30, 2026

Water → Methyl 5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylate

https://huagongshe.com/reaction/2174891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium AcetateHCID 517045—
Reactant2-Amino-4-(methoxycarbonyl)benzeneboronic acid hydrochlorideHCID 16427083—
ReactantMethyl 5-bromopyrimidine-4-carboxylateHCID 45790077—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylateHCID 509421448.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

Sodium acetate (4.0 eq, 1.92 g, 23.41 mmol) and 1,1′-bis(diphenylphosphino)ferrocene palladium (II) chloride (complexed with dichloromethane) (0.05 eq, 214 mg, 0.29 mmol) were added to a mixture of methyl-5-bromopyrimidine-4-carboxylate (1.0 eq, 1.27 g, 5.85 mmol), and 2-amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride (1.0 eq, 1.35 g, 5.85 mmol) in anhydrous DMF (10 ml). The Mixture was stirred under nitrogen atmosphere at 120° C. for 18 hours. Water and brine were added and the resulting solid impurities filtered off. The material was extracted with CH2Cl2 (4×) and the combined extracts dried over Na2SO4. After evaporation of CH2Cl2, the remaining DMF was evaporated by heating the residue in vacuo. The resulting solid was triturated in CH2Cl2, filtered and dried to provide methyl 5-oxo-5,6-dihydropyrimido[4,5-c]quinoline-8-carboxylate as a beige solid (127 mg, 8.5% yield). LCMS (ES): >80% pure, m/z 256 [M+1]+;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062043B2
Source datasetuspto-grants-2015_06
ORD IDord-2634948b445f4b73bb50fa1d6f5ac29b
Source noteuspto-grants-2015_06