HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466988Generated: November 2, 2026
HCID 66745563, compound → HCID 66746516, compound
https://huagongshe.com/reaction/1466988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66745563 | HCID 66745563 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 66746516 | HCID 66746516 | — |
Reaction Steps
Ethyl 4-(4-methoxybenzylamino)-2,5-dimethylquinoline-3-carboxylate (Example 12a, 0.563 g, 1.54 mmol) was dissolved in TFA (8 mL) and the resultant solution was stirred at room temperature for 15 minutes, TFA was then removed under vacuum to give the crude ethyl 4-amino-2,5-dimethylquinoline-3-carboxylate product, which was dissolved in EtOH (4 mL). To this solution was added NaOH (4.0 N, 3.86 mL) and the reaction mixture was stirred at 100° C. for 1 hr. Water (25 mL) was added, and the solvent was decanted away from insoluble material then acidified with AcOH to pH 5.5. The precipitate was collected by filtration to give the title compound (300 mg, 90%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 2.78 (s, 3H), 2.88 (s, 3H), 7.30 (d, J=7.2 Hz, 1H), 7.58 (d, J=8.0 Hz, 1H), 7.65 (m, 1H), 7.8-8.0 (br, 1H), 12.2-12.9 (br, 2H). MS 217 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000054B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-1796b5ea7e5f4d498a501c4a90874e7a |
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| Source note | uspto-grants-2015_04 |
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