HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392882Generated: October 29, 2026
Dimethylformamide → 2-(2-Phenyl-1,3-dioxan-5-yl)oxy-4-(3,4-methylenedioxybenzyl)amino-6-chloroquinazoline
https://huagongshe.com/reaction/2392882
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,3-Dioxan-5-ol, 2-phenyl- | HCID 74362 | — |
| Reactant | 4-((1,3-Benzodioxol-5-ylmethyl)amino)-2,6-dichloro quinazoline | HCID 22339865 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Phenyl-1,3-dioxan-5-yl)oxy-4-(3,4-methylenedioxybenzyl)amino-6-chloroquinazoline | HCID 57124416 | 27.8% |
Reaction Steps
100 mg of sodium hydride was added to a mixture comprising 300 mg of 5-hydroxy-2-phenyl-1,3-dioxane and 5 ml of dimethylformamide. The obtained mixture was heated to 80° C. After the bubbling had been discontinued, 300 mg of 2,6-dichloro-4-(3,4-methylenedioxybenzyl)aminoquinazoline was added in a crystalline state. The obtained mixture was heated at 140° C. for 2 hours and cooled, followed by the addition of water. The obtained mixture was extracted with ethyl acetate. The extract was purified by silica gel column chromatography using an ethyl acetate/benzene mixture to give 118 mg of 2-(2-phenyl-1,3-dioxan-5-yl)oxy-4-(3,4-methylenedioxybenzyl)amino-6-chloroquinazoline. 100 mg of this compound was hydrolyzed with concentrated hydrochloric acid/ethanol by a conventional process to give 60 mg of the title compound through rearrangement.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05801180 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-aa85e06b8c044c8eb39b7f5dc5eb0a24 |
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| Source note | uspto-grants-1998_09 |
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