HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 2-n-Butyl-4-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)semicarbazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Butylhydrazine | HCID 77064 | — |
| Reactant | 5-Methylsulfonyl-1,3,4-thiadiazol-2-yl isocyanate | HCID 54253736 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-n-Butyl-4-(5-methylsulfonyl-1,3,4-thiadiazol-2-yl)semicarbazide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007031 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-b3df16c51b864126ad4eb3a009ca7ce9 |
| Source note | uspto-grants-1977_02 |