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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579473Generated: October 27, 2026

Hydrazine → 1-Ethyl-N-(5-methyl-1,3,4-thiadiazol-2-yl)hydrazine-1-carboxamide

https://huagongshe.com/reaction/1579473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantEthylhydrazineHCID 29062—
Reactant2-Isocyanato-5-methyl-1,3,4-thiadiazoleHCID 54282028—
SolventDichloromethaneHCID 6344—
Product1-Ethyl-N-(5-methyl-1,3,4-thiadiazol-2-yl)hydrazine-1-carboxamideHCID 21454648—

Reaction Steps

A solution of ethylhydrazine (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-Methyl-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-ethyl-4-(5-methyl-1,3,4-thiadiazol-2-yl)semicarbazide as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931209
Source datasetuspto-grants-1976_01
ORD IDord-a643d4bb84f043a8b79bd6dccb4b773c
Source noteuspto-grants-1976_01