HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222585Generated: October 30, 2026
Hydrochloric Acid → N,3-Dihydroxypyridine-4-carboxamide
https://huagongshe.com/reaction/2222585
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Methyl 3-hydroxypyridine-4-carboxylate | HCID 12414071 | — |
| Product | N,3-Dihydroxypyridine-4-carboxamide | HCID 45123502 | 96% |
Reaction Steps
To a stirred suspension of methyl 3-hydroxy-isonicotinate (176 g; 1.15 mol) in water/ice (50/50, 1700 mL), was added hydroxylamine hydrochloride (127.9 g; 1.84 mol). The temperature fell to −5° C. and then aqueous NaOH solution (454 mL, 28% w/v) was added dropwise keeping the temperature below 5° C. during the addition. Hereafter the reaction mixture was stirred at ambient temperature for 1.5 h followed by heating to 60° C. At this temperature the pH was adjusted to 5.4 by the addition of aqueous hydrochloric acid (10 M) at which point a heavy precipitate forms. The reaction mixture was then stirred at ambient temperature followed by cooling to 5° C. The pH was then adjusted to 4.0 by the addition of aqueous hydrochloric acid (10 M), and then was stirred whilst cold for 1.5 h. The crystals were filtered off, rinsed with water (3×100 mL), dried on the filter and then dried further at reduced pressure and 40° C. overnight to give 3,N-dihydroxy-isonicotinamide (169.3 g, 96%; HPLC purity 98%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371863B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-0f18a5f623304a5c82ad161bb29e7190 |
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| Source note | uspto-grants-2008_05 |
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