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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117146Generated: October 26, 2026

Trifluoroacetic acid → 2-Oxo-1-(pyridin-2-yl)-1,2-dihydropyridine-3-carboxylic acid

https://huagongshe.com/reaction/2117146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-oxo-1-(pyridin-2-yl)-1,2-dihydropyridine-3-carboxylateHCID 21081726—
SolventMethanolHCID 887—
Product2-Oxo-1-(pyridin-2-yl)-1,2-dihydropyridine-3-carboxylic acidHCID 2108158655.4%

Reaction Steps

A mixture of methyl 2-oxo-1-(pyridin-2-yl)-1,2-dihydropyridine-3-carboxylate (500 mg, 2.17 mmol) and 3 N NaOH (1 mL) and methanol (10 mL) was stirred at rt overnight. To the reaction was added TFA (0.5 mL) and the mixture was concentrated in vacuo. The residue was dissolved in water (3 ML) and i-PrOH (10 mL). The solid which formed was filtered, washed with a small amount of water and i-PrOH, and dried to obtain the acid (260 mg, 55%) as a white solid. 1H NMR (DMF-d7) δ 14.14 (br s, 1H), 8.72 (d, 1H, J=4.9 Hz), 8.62 (dd, 1H, J=7.7, 2.2 Hz), 8.47 (dd, 1H, J=6.6, 2.2 Hz ), 8.18-7.98 (m, 2H), 7.67 (dd, 1H, J=7.2, 5.3 Hz), 6.97 (t, 1H, J=6.6 Hz); MS(ESI+) m/z 217.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439246B2
Source datasetuspto-grants-2008_10
ORD IDord-3ef2e2ed928a4aab87fd4e2e15105d01
Source noteuspto-grants-2008_10