HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047709Generated: October 31, 2026
Ammonia → Ethyl 4-amino-6-methoxyquinoline-3-carboxylate
https://huagongshe.com/reaction/2047709
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethyl 4-chloro-6-methoxyquinoline-3-carboxylate | HCID 304558 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Ethyl 4-amino-6-methoxyquinoline-3-carboxylate | HCID 16644472 | 92% |
Reaction Steps
A mixture of ethyl 4-chloro-6-methoxyquinoline-3-carboxylate (Example 1b, 796 mg, 3.0 mmol) and ammonia (25% aqueous solution, 10 mL) in isopropanol (40 mL) was stirred at 110° C. in a pressure reactor overnight. Most of the solvent was then removed under reduced pressure, and the reaction mixture was diluted with water. The precipitate was collected by filtration, washed with cold water, and dried under vacuum to give the title compound as an off-white solid (680 mg, 92%). 1H NMR (400 MHz, DMSO-d6) δ 1.33 (t, J=7.0 Hz, 3H), 3.88 (s, 3H), 4.32 (q, J=7.0 Hz, 2H), 7.36 (dd, J=2.8, 8.8 Hz, 1H), 7.72 (d, J=8.8 Hz, 1H), 7.74 (d, J=2.8 Hz, 1H), 8.23 (bs, 2H), 8.77 (s, 1H). MS 247 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592592B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-710350f9d416428cbf2cfd23edb8e0e9 |
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| Source note | uspto-grants-2013_11 |
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