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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantMethyl 3-hydroxypyridine-4-carboxylateHCID 12414071—
ProductN,3-Dihydroxypyridine-4-carboxamideHCID 4512350296%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371863B2
Source datasetuspto-grants-2008_05
ORD IDord-0f18a5f623304a5c82ad161bb29e7190
Source noteuspto-grants-2008_05