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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Diisocyanatobenzene | HCID 61009 | — |
| Reactant | 4-Dimethylamino-6-aminoquinaldine | HCID 17908882 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Dimethylamino-2-methylquinolin-6-yl)-3-{4-[3-(4-dimethylamino-2-methylquinolin-6-yl)ureido]phenyl}urea | HCID 12052465 | 48.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06995175B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-e61f52614bd343dab22c2e7bed72335e |
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| Source note | uspto-grants-2006_02 |
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