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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579476Generated: October 26, 2026

Hydrazine → N-(5-Methoxy-1,3,4-thiadiazol-2-yl)-1-propylhydrazine-1-carboxamide

https://huagongshe.com/reaction/1579476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantHydrazine, propyl-HCID 42007—
Reactant5-Methoxy-1,3,4-thiadiazol-2-yl isocyanateHCID 45123466—
SolventDichloromethaneHCID 6344—
ProductN-(5-Methoxy-1,3,4-thiadiazol-2-yl)-1-propylhydrazine-1-carboxamideHCID 21454627—

Reaction Steps

A solution of propylhydrazine (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-Methoxy-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-propyl-4-(5-methoxy-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-e0068004b9934841bb9455e8d58dc78f
Source noteuspto-grants-1976_01