HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887109Generated: October 25, 2026
Chloroacetic Acid → (5-Oxo-1,6-naphthyridin-6(5H)-YL)acetic acid
https://huagongshe.com/reaction/887109
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetic Acid | HCID 300 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,6-naphthyridin-5(6H)-one | HCID 5520368 | — |
| Product | (5-Oxo-1,6-naphthyridin-6(5H)-YL)acetic acid | HCID 57907423 | — |
Reaction Steps
To 1,6-naphthyridin-5(6H)-one (0.625 g, 4.28 mmol) was added 5 M sodium hydroxide solution (1.7 mL) followed by chloroacetic acid (0.404 g, 4.28 mmol). The reaction mixture was heated at 100° C. for 2 h. After cooled down to ambient temperature and neutralized with 2 N hydrochloric acid (2.1 mL), the title compound was collected by filtration as a yellow solid. 1H NMR (DMSO-d6): δ 13.1 (s, 1H), 8.94 (dd, J=4.6, 1.8 Hz, 1H), 8.51 (dd, J=8.0, 1.6 Hz, 1H), 7.72 (d, J=7.6 Hz, 1H), 7.52 (dd, J=8.0, 4.6 Hz, 1H), 6.72 (d, J=7.6 Hz, 1H), 4.72 (s, 2H). LC/MS 205.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247415B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-a0492798366f47e0935556308f54fdd0 |
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| Source note | uspto-grants-2012_08 |
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