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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579488Generated: October 31, 2026

Methylhydrazine → N-(5-Cyclobutyl-1,3,4-thiadiazol-2-yl)-1-methylhydrazine-1-carboxamide

https://huagongshe.com/reaction/1579488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantHydrazineHCID 9321—
Reactant5-Cyclobutyl-1,3,4-thiadiazol-2-yl isocyanateHCID 54345741—
SolventDichloromethaneHCID 6344—
ProductN-(5-Cyclobutyl-1,3,4-thiadiazol-2-yl)-1-methylhydrazine-1-carboxamideHCID 21454645—

Reaction Steps

A solution of methylhydrazine (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-Cyclobutyl-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-methyl-4-(5-cyclobutyl-1,3,4-thiadiazol-2-yl)semicarbazide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931209
Source datasetuspto-grants-1976_01
ORD IDord-6fb54ecde6ef4bb9b536c047bdfd6033
Source noteuspto-grants-1976_01