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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501041Generated: October 25, 2026

Triethylamine → 5-(5-Methoxy-benzofuran-2-yl)-pyridine-2-carboxylic acid amide

https://huagongshe.com/reaction/501041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Bromopyridine-2-carboxamideHCID 735151—
Reactant(5-Methoxy-1-benzofuran-2-yl)boronic acidHCID 22221596—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
Product5-(5-Methoxy-benzofuran-2-yl)-pyridine-2-carboxylic acid amideHCID 2501484128%

Reaction Conditions

Temperature140 °C

Reaction Steps

5-methoxybenzofuran boronic acid (1.2 mmol), 5-bromopyridine-2-carboxamide (1.0 mmol), Pd(PPh3)2Cl2 (0.024 mmol) and NEt3 (317 μL) were mixed in EtOH (10 mL) in a 20 mL microwave vial. The mixture was stirred at 140° C. for 10 min in a microwave reactor, filtered, and the precipitate was washed with water and EtOAc and dried under vacuum to afford the title compound (75 mg). 1H NMR δ ppm 9.10 (d, 1 H) 8.34 (dd, 1 H) 8.21 (br. s., 1 H) 8.00 (d, 1 H) 7.52-7.72 (m, 3 H) 7.25 (d, 1 H) 7.00 (dd, 1 H) 3.82 (s, 3H); MS m/z 269 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772256B2
Source datasetuspto-grants-2010_08
ORD IDord-75c556a2aa9943bda142118f08416f36
Source noteuspto-grants-2010_08