Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213827Generated: October 25, 2026

2,4-Dichloro-5-methoxyaniline → HCID 178486403, compound

https://huagongshe.com/reaction/2213827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-5-methoxyanilineHCID 1476636—
ReactantPyridinium chlorideHCID 10176127—
ReactantHCID 178486400HCID 178486400—
SolventGlycol monoethyl etherHCID 8076—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178486403HCID 17848640365.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 0.7 g (2.46 mmol) of 4-chloro-8-hydroxy-7-methoxybenzo[g]quinoline-3-carbonitrile, 0.57 g (2.95 mmol) of 2,4-dichloro-5-methoxyaniline and 0.28 g (2.46 mmol) of pyridine hydrochloride in 7 mL of 2-ethoxyethanol is heated at 120° C. for 2 hours, then cooled to room temperature. The product mixture is diluted with saturated solution of sodium bicarbonate and stirred for 15 minutes. The resulting solid is collected by filtration, washed with water and dried. The crude product is purified by silica gel chromatography, utilizing a 98:2 to 90:10 gradient of methylene chloride/methanol to give 0.71 g of 4-(2,4-dichloro-5-methoxyphenylamino)-8-hydroxy-7-methoxybenzo[g]quinoline-3-carbonitrile as a yellow solid, mp, 238–240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105531B2
Source datasetuspto-grants-2006_09
ORD IDord-5e1cc48af3284ba49d124e503bd5f601
Source noteuspto-grants-2006_09