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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346417Generated: October 25, 2026

3-Morpholino-1-propanol → 4-[(3,4-Dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazoline

https://huagongshe.com/reaction/346417

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Morpholino-1-propanolHCID 199576—
ReactantSodiumHCID 5360545—
Reactant4-[(3,4-Dichloro-6-fluorophenyl)amino]-7-fluoro-6-nitroquinazolineHCID 11176185—
SolventTetrahydrofuranHCID 8028—
Product4-[(3,4-Dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazolineHCID 2108000172%

Reaction Conditions

Temperature20 °C

Reaction Steps

Sodium metal (5 equivalents) was added, under nitrogen atmosphere, to a solution of 3-(4-morpholinyl)-1-propanol (4 equivalents) in THF. The obtained suspension was stirred at 20° C. for two hours and was thereafter cannulated, under nitrogen atmosphere, into a solution of 4-[(3,4-dichloro-6-fluorophenyl)amino]-7-fluoro-6-nitroquinazoline. The reaction mixture was refluxed for 18 hours, the solvent was thereafter partially removed under reduced pressure and the residue was diluted with water and extracted with ethyl acetate. Drying the combined organic extracts, evaporation and silica gel chromatography (using a mixture of 20% MeOH/30% CH2Cl2/50% EtOAc as elute) gave 4-[(3,4-dichloro-6-fluorophenyl)amino]-7-[3-(4-morpholinyl)propoxy]-6-nitroquinazoline in 72% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07172749B2
Source datasetuspto-grants-2007_02
ORD IDord-44f5507bc07f4cd99812ba644cbcabc3
Source noteuspto-grants-2007_02