HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302242Generated: October 31, 2026
Diisopropylethylamine → HCID 22057962, compound
https://huagongshe.com/reaction/2302242
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Quinolinecarboxylic acid | HCID 82571 | — |
| Reactant | HCID 22057981 | HCID 22057981 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22057962 | HCID 22057962 | 24.4% |
Reaction Steps
6-Quinolinecarboxylic acid (0.173 g) was added to a stirred suspension of N-(3-amino4-methylphenyl)3-dimethylaminobenzamide (0.135 g), diisopropylethylamine (0.325 ml), 2-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate(V) (0.39 g) in DMF (10 ml) and the resultant mixture was stirred at ambient temperature for 16 hours. The solvent was evaporated and the residue was dissolved in methylene chloride and washed with a saturated aqueous sodium bicarbonate solution, dried over magnesium sulphate and evaporated. The residue was triturated under a mixture of ethyl acetate and isohexane. There was thus obtained the title compound as a solid (0.052 g); NMR Spectrum: (DMSOd6) 2.24 (s, 3H), 2.95 (s, 6H), 6.89 (d, 1H), 7.25 (m, 4H), 7.6 (m, 2H), 7.85 (s, 1H), 8.12 (d, 1H), 8.4 (d, 1H), 8.52 (d, 1H), 8.65 (m, 1H), 8.99 (d, 1H), 10.11 (s, 1H), 10.16 (s, 1H); Mass Spectrum: M+H+ 425.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06432949B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-24b4cba271664471a651b102cdc50b24 |
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| Source note | uspto-grants-2002_08 |
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