HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241570Generated: October 31, 2026
Water → 7-Hydroxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinazoline
https://huagongshe.com/reaction/1241570
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 7-Benzyloxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinazoline hydrochloride | HCID 21936097 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Hydroxy-6-methoxy-4-(2,3-methylenedioxyanilino)quinazoline | HCID 135594113 | 100.5% |
Reaction Steps
A mixture of 7-benzyloxy-6-methoxy-4-(2,3methylenedioxyanilino)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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115615B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-11fc6ca0af324211b8e0c0db76b39ee4 |
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| Source note | uspto-grants-2006_10 |
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