HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178641Generated: November 1, 2026
4-Formylphenylboronic Acid → HCID 10343928, compound
https://huagongshe.com/reaction/1178641
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Formylphenylboronic Acid | HCID 591073 | — |
| Reactant | 7-[(2,4-Dichloro-5-methoxyphenyl)amino]-2-iodothieno[3,2-b]pyridine-6-carbonitrile | HCID 10390208 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 10343928 | HCID 10343928 | 70.4% |
Reaction Steps
A mixture of 7-[(2,4-dichloro-5-methoxyphenyl)amino]-2-iodothieno[3,2-b]pyridine-6-carbonitrile (240 mg, 0.50 mmol), 4-formylphenylboronic acid (150 mg, 1.0 mmol) and 4 mg of tetrakis(triphenylphosphine)palladium(0) in 20 mL of ethylene glycol dimethyl ether and 16 mL of saturated aqueous sodium bicarbonate is heated at reflux for 2 hours. The reaction mixture is cooled to room temperature and partitioned between water and ethyl acetate. The organic layer is dried over sodium sulfate, filtered and concentrated in vacuo. The residue is purified by flash column chromatography eluting with chloroform to provide 160 mg of 7-[(2,4-dichloro-5-methoxyphenyl)amino]-2-(4-formylphenyl)thieno[3,2-b]pyridine-6-carbonitrile as yellow crystals, mp 261–262°°C.; 1H NMR (DMSO-d6) δ 3.87 (s, 3H), 7.41 (s, 1H), 7.63 (s, 1H), 7.90–8.03 (m, 4H), 8.15 (s, 1H), 8.65 (s, 1H), 9.83 (s, 1H), 10.05 (s, 1H); MS 454.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07276519B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-5f2ba39b76544df5b9a775a9dab94fb0 |
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| Source note | uspto-grants-2007_10 |
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