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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611498Generated: October 26, 2026

4-Formylphenylboronic Acid → 7-Chloro-2-(4-formylphenyl)thieno[3,2-b]pyridine-6-carbonitrile

https://huagongshe.com/reaction/1611498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Formylphenylboronic AcidHCID 591073—
Reactant7-Chloro-2-iodothieno[3,2-B]pyridine-6-carbonitrileHCID 9996143—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventSodium BicarbonateHCID 516892—
Product7-Chloro-2-(4-formylphenyl)thieno[3,2-b]pyridine-6-carbonitrileHCID 1146074587.8%

Reaction Steps

A mixture of 7-chloro-2-iodo-thieno[3,2-b]pyridine-6-carbonitrile (1.00 g, 3.12 mmol), 4-formylphenylboronic acid (936 mg, 6.24 mmol) and 108 mgs of tetrakis(triphenylphosphine)palladium(0) in 30 mL of ethylene glycol dimethyl ether and 25 mL of aqueous saturated sodium bicarbonate is heated at reflux for 4 hours. The mixture is cooled and the precipitate is collected by filtration washing with ethyl acetate and diethyl ether to provide 818 mg of 7-chloro-2-(4-formylphenyl)thieno[3,2-b]pyridine-6-carbonitrile as a yellow solid, mp 300-305° C.; 1H NMR (CDCl3) δ 7.93 (d, J=8 Hz, 2H), 7.96 (s, 1H), 8.03 (d, J=8 Hz, 2H), 8.87 (s, 1H), 10.1 (s, 1H), MS 298.0, 300.0 (M−H)−H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06987116B2
Source datasetuspto-grants-2006_01
ORD IDord-d77f85ad4781437b9fbe9e05daa9d34e
Source noteuspto-grants-2006_01