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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900676Generated: October 30, 2026

Dimethylformamide → 2-(2-Phenyl-1,3-dioxan-5-yl)oxy-4-(3,4-methylenedioxybenzyl)amino-6-chloroquinazoline

https://huagongshe.com/reaction/1900676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant1,3-Dioxan-5-ol, 2-phenyl-HCID 74362—
Reactant4-((1,3-Benzodioxol-5-ylmethyl)amino)-2,6-dichloro quinazolineHCID 22339865—
SolventWaterHCID 962—
Product2-(2-Phenyl-1,3-dioxan-5-yl)oxy-4-(3,4-methylenedioxybenzyl)amino-6-chloroquinazolineHCID 5712441627.8%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576322
Source datasetuspto-grants-1996_11
ORD IDord-4b86575e9649499bbe8b39a242ad1d0a
Source noteuspto-grants-1996_11