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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381861Generated: November 3, 2026

3-Pyridinemethanamine → 5-(5-benzyl-1H-1,2,4-triazol-3-yl)-3-methyl-N-(pyridin-3-ylmethyl)thiophene-2-carboxamide

https://huagongshe.com/reaction/2381861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinemethanamineHCID 31018—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5-(5-benzyl-1H-1,2,4-triazol-3-yl)-3-methylthiophene-2-carboxylic acidHCID 59179713—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-(5-benzyl-1H-1,2,4-triazol-3-yl)-3-methyl-N-(pyridin-3-ylmethyl)thiophene-2-carboxamideHCID 2495785567%

Reaction Steps

To a stirred mixture of 5-(5-benzyl-1H-1,2,4-triazol-3-yl)-3-methylthiophene-2-carboxylic acid (0.13 g, 0.43 mmol), 1-hydroxybenzotriazole (0.088 g, 0.65 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.13 g, 0.65 mmol) in anhydrous N,N-dimethylformamide (2 mL) was added N,N-diisopropylethylamine (0.23 mL, 1.30 mmol), followed by the addition of 3-(aminomethyl)pyridine (0.044 mL, 0.44 mmol). The resulting reaction mixture was stirred at ambient temperature for 18 h, and diluted with ethyl acetate (75 mL). The organic layer was washed with saturated aqueous sodium bicarbonate (3×35 mL) and water (35 mL), dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography eluted with 10% methanol in dichloromethane to afford the title compound as a colorless foam (0.11 g, 67%): mp 82° C. (dec.); 1H NMR (300 MHz, DMSO-d6) δ 8.66 (t, J=5.6 Hz, 1H), 8.55 (s, 1H), 8.46 (s, 1H), 7.73 (d, J=7.9 Hz, 1H), 7.42-7.20 (m, 8H), 4.44 (d, J=5.6 Hz, 2H), 4.10 (s, 2H), 2.43 (s, 3H); MS (ES+) m/z 390.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258160B2
Source datasetuspto-grants-2012_09
ORD IDord-24cfe45382cd44768457ff343c84c569
Source noteuspto-grants-2012_09