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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Terephthalic Acid | HCID 7489 | — |
| Reactant | 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride | HCID 2734059 | — |
| Reactant | 4-Dimethylamino-6-aminoquinaldine | HCID 17908882 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | N,N'-bis(4-dimethylamino-2-methylquinolin-6-yl)-terephthalamide | HCID 12052464 | 99.7% |
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
| 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-860eb2daabb54d0aa8d3495620a4260b |
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| Source note | uspto-grants-2006_02 |
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