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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365761Generated: November 1, 2026

Triethylamine → 4-(2-Aminobenzylamino)-7-ethylamino-6-nitroquinazoline

https://huagongshe.com/reaction/365761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(Aminomethyl)anilineHCID 178096—
Reactant4-Chloro-7-ethylamino-6-nitroquinazolineHCID 23292989—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Aminobenzylamino)-7-ethylamino-6-nitroquinazolineHCID 2329301378.1%

Reaction Steps

4-Chloro-7-ethylamino-6-nitroquinazoline (5.00 g, 19.8 mmol), triethylamine (8.3 ml, 60.9 mmol), and 2-aminobenzylamine (2.9 g, 23.8 mmol) were stirred at room temperature overnight in tetrahydrofuran. After the reaction was completed, the solution was concentrated under reduced pressure, and the resulting solids were washed with methanol to give the title compound (5.23 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127541
Source datasetuspto-grants-2000_10
ORD IDord-faac0658e24944a9adef8d8190e97f56
Source noteuspto-grants-2000_10