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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051233Generated: November 2, 2026

Benzenamine, 3-ethynyl- → N-(3-ethynylphenyl)-7-fluoro-6-nitroquinazolin-4-amine

https://huagongshe.com/reaction/1051233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenamine, 3-ethynyl-HCID 104682—
Reactant4-Chloro-7-fluoro-6-nitroquinazolineHCID 10609358—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductN-(3-ethynylphenyl)-7-fluoro-6-nitroquinazolin-4-amineHCID 5914275951.2%

Reaction Steps

To a solution of 4-chloro-7-fluoro-6-nitroquinazoline (12 g, 0.052 mol) in 120 mL DCM in an ice bath was added slowly a solution of 3-ethynylaniline (7 g, 0.060 mol) in 200 mL isopropanol. The reaction solution was stirred for 1 hour, then TEA (7 g, 0.069 mol) was added and stirred for another 0.5 hour at room temperature. The resulting solid precipitate was filtered and washed with 20 mL isopropanol twice, 20 mL H2O for twice, and dried to give N-(3-ethynylphenyl)-7-fluoro-6-nitroquinazolin-4-amine as yellow solid 8.2 g (50.3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388170B2
Source datasetuspto-grants-2016_07
ORD IDord-263c52c7d7c04fe7ba0d379bedb81f1a
Source noteuspto-grants-2016_07