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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371476Generated: October 31, 2026

Water → 7-Hydroxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinazoline

https://huagongshe.com/reaction/1371476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium formateHCID 2723923—
Reactant7-Benzyloxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinazoline hydrochlorideHCID 21936097—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
Product7-Hydroxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinazolineHCID 135594113100.5%

Reaction Steps

A mixture of 7-benzyloxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinazoline hydrochloride (21 g), ammonium formate (30.2 g), 10% palladium-on-charcoal catalyst (4.8 g), water (26 ml) and DMF (350 ml) was stirred at ambient temperature for 2 hours. The mixture was filtered and the filtrate was evaporated. The residual oil was triturated under diethyl ether. The solid so obtained was triturated under water, collected by filtration, washed with water and with diethyl ether and dried under vacuum over phosphorus pentoxide. The material so obtained was purified by column chromatography on silica using a 9:1 mixture of methylene chloride and methanol as eluent. There was thus obtained the title compound (15 g); NMR Spectrum: (DMSOd6) 3.95 (s, 3H), 6.0 (s, 2H), 6.85 (m, 2H), 6.95 (d, 1H), 7.05 (s, 1H), 7.8 (s, 1H), 8.3 (s, 1H), 9.4 (s, 1H), 10.3 (s, 1H); Mass Spectrum: M+H+ 312.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157467B2
Source datasetuspto-grants-2007_01
ORD IDord-77491d44b5eb4693b45fe34e8755fe37
Source noteuspto-grants-2007_01