HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410146Generated: October 31, 2026
Sodium Hydroxide → 4-Amino-6-methoxyquinoline-3-carboxylic acid
https://huagongshe.com/reaction/2410146
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-amino-6-methoxyquinoline-3-carboxylate | HCID 16644472 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Amino-6-methoxyquinoline-3-carboxylic acid | HCID 16644490 | 93% |
Reaction Steps
To a stirred solution of ethyl 4-amino-6-methoxyquinoline-3-carboxylate (Example Aa, 1.23 g, 5.0 mmol) in EtOH (20.0 mL) was added aqueous NaOH (2.0 N, 5.0 mL) at room temperature. The reaction mixture was then refluxed for 3 hr. The solution was then filtered and washed with water. The filtrate was cooled to 0° C. and neutralized carefully with 1 N HCl to pH 7. Most of the EtOH was removed under reduced pressure, and the precipitate was collected by filtration, washed with cold water, and dried under vacuum to give the title compound as an off-white solid (1.01 g, 93%). 1H NMR (400 MHz, DMSO-d6) δ 3.89 (s, 3H), 7.40 (dd, J=2.8, 9.4 Hz, 1H), 7.73 (d, J=9.4 Hz, 1H), 7.77 (d, J=2.8 Hz, 1H), 8.77 (s, 1H). MS 219 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815956B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-889b5b7cb7184a9ca1cece9ab69f77ce |
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| Source note | uspto-grants-2014_08 |
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