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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364527Generated: October 31, 2026

Ethanol → 3-(Cyclopropylamino)-5-[(4-fluorophenyl)methyl]-2-pyridinecarboxylic acid

https://huagongshe.com/reaction/2364527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant3-(Cyclopropylamino)-5-[(4-fluorophenyl)methyl]-2-pyridinecarbonitrileHCID 69482186—
Product3-(Cyclopropylamino)-5-[(4-fluorophenyl)methyl]-2-pyridinecarboxylic acidHCID 6948047799%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 3-(cyclopropylamino)-5-[(4-fluorophenyl)methyl]-2-pyridinecarbonitrile (360 mg, 1.34 mmol) in ethanol (25 mL) was treated with sodium hydroxide (2 mL, 50% aqueous) and heated at 100° C. (bath temperature) for 14 hours. The reaction mixture was concentrated in vacuo and the residue taken up in water and cooled in an ice bath. The solution was acidified by the slow addition of 6 NHCl (final pH˜3). The aqueous layer was extracted with ethyl acetate and the organics dried over sodium sulfate. Filtration and concentration gave 3-(cyclopropylamino)-5-[(4-fluorophenyl)methyl]-2-pyridinecarboxylic acid (385 mg, 99%) as a white powder. 1H NMR (400 MHz, CDCl3) δ 8.94 (br, 1 H), 7.93 (s, 1 H), 7.74 (s, 1 H), 7.30 (s, 1 H), 7.15 (dd, J=8.5, 5.5 Hz, 2 H), 7.00 (t, J=8.7 Hz, 2 H), 3.97 (s, 2 H), 2.40 (m, 1 H), 0.77 (m, 2 H), 0.54 (m, 2 H); MS m/z 287 M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691991B2
Source datasetuspto-grants-2014_04
ORD IDord-63489ddf97944f85a68cdbb92e113b49
Source noteuspto-grants-2014_04