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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435907Generated: October 26, 2026

Hydrazine → 2-n-Butyl-4-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)semicarbazide

https://huagongshe.com/reaction/435907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantButylhydrazineHCID 77064—
Reactant5-Methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanateHCID 54253736—
SolventDichloromethaneHCID 6344—
Product2-n-Butyl-4-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)semicarbazideHCID 21454625—

Reaction Steps

A solution of n-butylhydrazine (0.3 mole) in methylene chloride (150 ml) is charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 5-Methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanate dimer (0.1 mole) is then added, with stirring, at room temperature. After the addition is completed the reaction mixture is heated at reflux for a period of about 4 hours. After this time the reaction mixture is stripped of solvent and excess hydrazine to yield the desired product 2-n-butyl-4-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)semicarbazide as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04007031
Source datasetuspto-grants-1977_02
ORD IDord-b3df16c51b864126ad4eb3a009ca7ce9
Source noteuspto-grants-1977_02