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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611511Generated: November 1, 2026

Water → 7-[(2,4-Dichlorophenoxy)]thieno[3,2-b]pyridine-6-carbonitrile

https://huagongshe.com/reaction/1611511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,4-DichlorophenolHCID 8449—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Chlorothieno[3,2-b]pyridine-6-carbonitrileHCID 11816401—
SolventDimethylformamideHCID 6228—
Product7-[(2,4-Dichlorophenoxy)]thieno[3,2-b]pyridine-6-carbonitrileHCID 1001896373.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 7-chlorothieno[3,2-b]pyridine-6-carbonitrile (200 mg, 1.03 mmol), potassium carbonate (194.9 mg, 1.41 mmol) and 2,4-dichlorophenol (218.3 mg, 1.34 mmol) in 3 mL of N,N-dimethylformamide is stirred at 110° C. for 4 hours and allowed to cool to ambient temperature. The reaction mixture is treated with water and stirred at ambient temperature for 10 minutes. The crude solid is collected by filtration washing with water, dried in vacuo, then purified by flash column chromatography eluting with a gradient of 5% ethyl acetate in hexane to 20% ethyl acetate in hexane to provide 244 mg of 7-[(2,4-dichlorophenoxy)]thieno[3,2-b]pyridine-6-carbonitrile as a white solid, mp 158-160° C.; 1H NMR (DMSO-d6) δ 7.63 (dd, J=6, 2 Hz, 1H), 7.68 (d, J=4 Hz, 1H), 7.74 (d, J=6 Hz, 1H), 7.80 (d, J=2 Hz, 1H), 8.33 (d, J=4 Hz, 1H), 9.03 (s, 1H); MS 320.9, 322.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06987116B2
Source datasetuspto-grants-2006_01
ORD IDord-9ad008cfa5d04ae0a614cb656b528d40
Source noteuspto-grants-2006_01