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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxyanilineHCID 32285—
ReactantSodium BicarbonateHCID 516892—
ReactantPyridinium chlorideHCID 10176127—
ReactantHCID 22256673HCID 22256673—
SolventGlycol monoethyl etherHCID 8076—
ProductHCID 10344502HCID 1034450285.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06987116B2
Source datasetuspto-grants-2006_01
ORD IDord-d5e2c3ef95344fb4b4ac54ce9d82bc9a
Source noteuspto-grants-2006_01