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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579489Generated: November 1, 2026

Formaldehyde → 4-(5-Cyclobutyl-1,3,4-thiadiazol-2-yl)-2-methyl-1,2,4-triazolidin-3-one

https://huagongshe.com/reaction/1579489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPotassium HydroxideHCID 14797—
ReactantN-(5-Cyclobutyl-1,3,4-thiadiazol-2-yl)-1-methylhydrazine-1-carboxamideHCID 21454645—
SolventMethanolHCID 887—
Product4-(5-Cyclobutyl-1,3,4-thiadiazol-2-yl)-2-methyl-1,2,4-triazolidin-3-oneHCID 21454643—

Reaction Steps

2-Methyl-4-(5-cyclobutyl-1,3,4-thiadiazol-2-yl)-semicarbazide (0.1 mole) dissolved in methanol (100 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. Aqueous formaldehyde (0.2 mole; 37% concentration) is then added to the reaction vessel with stirring. Dilute aqueous potassium hydroxide is added to the reaction mixture to adjust the pH to between 7 and 8 and stirring is continued for a period of about 20 minutes resulting in the formation of a solid precipitate. The precipitate is recovered by filtration, is recrystallized and is dried under vacuum to yield the desired product 2-methyl-4-(5-cyclobutyl-1,3,4-thiadiazol-2-yl)-1,2,4-triazolidin-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931209
Source datasetuspto-grants-1976_01
ORD IDord-84ec292d6b1d40ad806ec2fef1df1d9f
Source noteuspto-grants-1976_01