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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588477Generated: November 3, 2026

1,4-Dioxane → HCID 178508856, compound

https://huagongshe.com/reaction/1588477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 54082773HCID 54082773—
SolventSodium HydroxideHCID 14798—
ProductHCID 178508856HCID 178508856—

Reaction Conditions

Temperature24 °C

Reaction Steps

A suspension of 0.4 g (1.2 mM) of 2,4-diamino-6-[2-(3,5-dichlorophenyl)ethenyl]pyrido[2,3-d]pyrimidine (prepared as described in Example 3), in 80 ml of 1N sodium hydroxide was heated at reflux for 24 hours. Since not all the starting material had dissolved, 10 ml of 5N sodium hydroxide and 25 ml of dioxane were added, and the mixture was heated at reflux for an additional 24 hours. The reaction mixture was cooled to 24° C., filtered, and the filtrate was diluted with 30 ml of glacial acetic acid. The precipitate which formed was collected by filtration, washed with 50 ml of water, and then with 50 ml of diethyl ether, and dried at 100° C. under vacuum to provide 160 mg of 2-amino-4-hydroxy-6-[2-(3,5-dichlorophenyl)ethenyl]pyrido-[2,3-d]pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05223503
Source datasetuspto-grants-1993_06
ORD IDord-10338759828a4d47936aa59e7040e3c9
Source noteuspto-grants-1993_06