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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970940Generated: October 25, 2026

Picolinic acid → Pyridine-2-carboxylic acid 4-hydroxymethyl-benzylamide

https://huagongshe.com/reaction/970940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant[4-(Aminomethyl)phenyl]methanolHCID 6496943—
SolventDimethylformamideHCID 6228—
ProductPyridine-2-carboxylic acid 4-hydroxymethyl-benzylamideHCID 2260129295%

Reaction Steps

Using General Procedure F: To a stirred solution of 4-aminomethylbenzyl alcohol (203 mg, 1.48 mmol) in DMF (3 mL) was added picolinic acid (198 mg, 1.61 mmol), 1-hydroxybenzotriazole (213 mg, 1.58 mmol), N,N-diisopropylethylamine (0.39 mL, 2.24 mmol) and 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide HCl (EDC) (315 mg, 1.64 mmol) and the mixture stirred overnight at room temperature. Standard work-up afforded the title compound (340 mg, 95%) as a yellow oil. 1H NMR (300 MHz, CDCl3) δ 4.67 (d, 2H, J=6.0 Hz), 4.69 (s, 2H), 7.36 (br s, 4H), 7.43-7.44 (m, 1H), 7.85-7.86 (m, 1H), 8.24 (d, 1H, J=9.0 Hz), 8.52 (br s, 1H), 8.52 (d, 1H, J=3.0 Hz). ES-MS m/z 243 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312234B2
Source datasetuspto-grants-2007_12
ORD IDord-d31189298b614c27bd5180ff456da0a3
Source noteuspto-grants-2007_12