HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → N-(5-Methoxy-1,3,4-thiadiazol-2-yl)-1-propylhydrazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Hydrazine, propyl- | HCID 42007 | — |
| Reactant | 5-Methoxy-1,3,4-thiadiazol-2-yl isocyanate | HCID 45123466 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(5-Methoxy-1,3,4-thiadiazol-2-yl)-1-propylhydrazine-1-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007031 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-5278aac87e224c37aed868ec31f8f32f |
| Source note | uspto-grants-1977_02 |