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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1900673Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1900673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktBoron TrichlorideHCID 25135—
Edukt4-((3,4-(Methylenedioxy)benzyl)amino)-6,7,8-trimethoxyquinazolineHCID 205964—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(3,4-Dihydroxybenzyl)amino-6,7,8-trimethoxyquinazoline hydrochlorideHCID 18796743—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05576322
Quelldatensatzuspto-grants-1996_11
ORD IDord-e35fd79631004756be87527bde643883
Quellennotizuspto-grants-1996_11