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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900673Generated: October 26, 2026

Methanol → 4-(3,4-Dihydroxybenzyl)amino-6,7,8-trimethoxyquinazoline hydrochloride

https://huagongshe.com/reaction/1900673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron TrichlorideHCID 25135—
Reactant4-((3,4-(Methylenedioxy)benzyl)amino)-6,7,8-trimethoxyquinazolineHCID 205964—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product4-(3,4-Dihydroxybenzyl)amino-6,7,8-trimethoxyquinazoline hydrochlorideHCID 18796743—

Reaction Steps

30 ml of a 1.0M solution of boron trichloride in methylene chloride was dropped into a solution of 2.00 g (5.41 mmol) of 4-(3,4-methylenedioxybenzyl)amino-6,7,8-trimethoxyquinazoline in 150 ml of chloroform under stirring at room temperature. The obtained mixture was stirred at room temperature for 2 days, followed by the addition of methanol and the obtained mixture was distilled under a reduced pressure to remove the solvent. This procedure was repeated thrice and the obtained residue was purified by silica gel column chromatography (chloroform/n-hexane). Hydrochloric acid/ethanol was added to the eluate and the obtained mixture was distilled under a reduced pressure to remove the solvent, followed by the addition of ethanol. The crystals thus formed were recovered by filtration. Thus, 0.59 g of the title compound was obtained as a colorless needle.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576322
Source datasetuspto-grants-1996_11
ORD IDord-e35fd79631004756be87527bde643883
Source noteuspto-grants-1996_11