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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890250Generated: October 30, 2026

1,4-Diisocyanatobenzene → 1-(4-Dimethylamino-2-methylquinolin-6-yl)-3-{4-[3-(4-dimethylamino-2-methylquinolin-6-yl)ureido]phenyl}urea

https://huagongshe.com/reaction/890250

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DiisocyanatobenzeneHCID 61009—
Reactant4-Dimethylamino-6-aminoquinaldineHCID 17908882—
SolventDimethylformamideHCID 6228—
Product1-(4-Dimethylamino-2-methylquinolin-6-yl)-3-{4-[3-(4-dimethylamino-2-methylquinolin-6-yl)ureido]phenyl}ureaHCID 1205246548.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 25 mg of 1,4-phenylene diisocyanate and 62.8 mg of 6-amino-4-dimethylamino-2-methylquinoline in 1 mL of dimethylformamide is stirred at a temperature in the region of 20° C. for 5 hours. 2 mL of dimethylformamide, 218 mg of polystyrene-isocyanate resin (Argonaut, 1.49 mmol/g) and 42 mg of polystyrene-trisamine resin (Argonaut, 3.75 mmol/g) are then added to the reaction mixture. The suspension obtained is stirred at a temperature in the region of 20° C. for 17 hours, filtered on sintered glass, and then the solid residue is washed with 10 mL of a dichloromethane-methanol (90-10 by volume) mixture. The filtrate obtained is concentrated under air stream at a temperature in the region of 50° C. 42.4 mg of 1-(4-dimethylamino-2-methylquinolin-6-yl)-3-{4-[3-(4-dimethylamino-2-methylquinolin-6-yl)ureido]phenyl}urea are thus obtained in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995175B2
Source datasetuspto-grants-2006_02
ORD IDord-e61f52614bd343dab22c2e7bed72335e
Source noteuspto-grants-2006_02