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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889150Generated: October 30, 2026

4-Aminotetrahydropyran → 5-Methyl-4-(tetrahydropyran-4-yl)-2,4-dihydro[1,2,4]triazol-3-one

https://huagongshe.com/reaction/889150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminotetrahydropyranHCID 419223—
Reactant5-Methyl-2,3-dihydro-1,3,4-oxadiazol-2-oneHCID 5323974—
SolventMethanolHCID 887—
Product5-Methyl-4-(tetrahydropyran-4-yl)-2,4-dihydro[1,2,4]triazol-3-oneHCID 5792738643.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

After dissolving 5-methyl-3H-[1,3,4]oxadiazol-2-one (CAS 3069-67-8) (500 mg) in methanol (5 ml), 4-aminotetrahydropyran (1.01 g) was added and the mixture was heated to reflux for 15 hours. The reaction mixture was concentrated under reduced pressure, and then a 1N aqueous solution of sodium hydroxide (5.5 ml) was added to the residue and the mixture Was stirred at 100° C. for 2 hours. After then adding 5N hydrochloric acid (1.1 ml) to the reaction mixture, it was stirred at room temperature for 3 hours. The precipitate was collected by filtration and washed with water and ethyl acetate in that order to obtain the title compound (400 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252810B2
Source datasetuspto-grants-2012_08
ORD IDord-d5505177918c4e67927e54600b11ac7c
Source noteuspto-grants-2012_08