HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611544Generated: October 30, 2026
3,4,5-Trimethoxyaniline → HCID 10344502, compound
https://huagongshe.com/reaction/1611544
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4,5-Trimethoxyaniline | HCID 32285 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | HCID 22256673 | HCID 22256673 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | HCID 10344502 | HCID 10344502 | 85.7% |
Reaction Steps
A mixture of 3,4,5-trimethoxyaniline (964 mg, 5.26 mmol), pyridine hydrochloride (100 mg, 0.76 mmol) and 4-chloro-2-iodothieno[3,2-b]pyridine-6-carbonitrile (937 mg, 2.92 mmol) in 50 mL of 2-ethoxyethanol is heated at reflux overnight. The solution is poured into saturated aqueous sodium bicarbonate and the resulting solid is collected by filtration, washed with water and dried under reduced pressure. The resultant solid is purified by flash column chromatography eluting with 2% methanol in dichloromethane. The fractions containing product are combined and concentrated to provide 1.17 g of 2-iodo-7-[(3,4,5-trimethoxyphenyl)amino]thieno[3,2-b]pyridine-6-carbonitrile as white crystals, mp 254-256° C.; 1H NMR (DMSO-d6) δ 3.70-3.78 (m, 9H), 6.66 (s, 2H), 7.72 (s, 1H), 8.53 (s, 1H), 9.56 (s, 1H); MS 468.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06987116B2 |
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| Source dataset | uspto-grants-2006_01 |
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| ORD ID | ord-d5e2c3ef95344fb4b4ac54ce9d82bc9a |
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| Source note | uspto-grants-2006_01 |
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