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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890249Generated: October 29, 2026

Terephthalic Acid → N,N'-bis(4-dimethylamino-2-methylquinolin-6-yl)-terephthalamide

https://huagongshe.com/reaction/890249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTerephthalic AcidHCID 7489—
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
Reactant4-Dimethylamino-6-aminoquinaldineHCID 17908882—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventDiisopropyl EtherHCID 7914—
ProductN,N'-bis(4-dimethylamino-2-methylquinolin-6-yl)-terephthalamideHCID 1205246499.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

4-(4,6-Dimethoxy-1,3,5-triazine-2-yl)-4-methylmorpholinium chloride (177 mg) is added to a solution of 48 mg (0.29 mmol) of terephthalic acid and 128 mg (0.64 mmol) of 4-dimethylamino-6-aminoquinaldine in 6 mL of dimethylformamide, at a temperature in the region of 20° C. The mixture obtained is stirred at a temperature in the region of 20° C. for about 12 hours. The reaction mixture is successively taken up in 2 mL of acetonitrile and 2 mL of diisopropyl ether, and the precipitate thus obtained is slowly filtered on a 6 mL BOND-ELUT cartridge filled with sintered material. The insoluble matter obtained is washed with diisopropyl ether and then dried under argon. 154 mg of N,N′-bis(4-dimethylamino-2-methylquinolin-6-yl)-terephthalamide are thus obtained in the form of a beige powder of whose characteristics are the following:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995175B2
Source datasetuspto-grants-2006_02
ORD IDord-860eb2daabb54d0aa8d3495620a4260b
Source noteuspto-grants-2006_02