HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine hydrate (1:1) → N-(5-Amino-1,2,4-triazol-3-yl)-2,5-dichlorobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 178503936 | HCID 178503936 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(5-Amino-1,2,4-triazol-3-yl)-2,5-dichlorobenzenesulfonamide | HCID 13772881 | 63.2% |
Reaction Steps
A mixture of 8.51 g (26.2 mmol) of N'-cyano-N-(2,5-dichlorophenylsulfonyl)-S-methylisothiourea and 10 ml (10 g, 0.20 mol) of hydrazine monohydrate in 85 ml of ethanol was heated at reflux for 30 minutes. After cooling to room temperature, the solid which separated was collected and suspended in 170 ml of H2O and the suspension was acidified with concentrated aqueous HCl. After stirring the suspension for 4 hours the solid was collected and dried in vacuo to yield 5.10 g (57 percent) of the desired product as a hydrochloride salt, mp 306°-308° C. IR and 1H NMR spectra were consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04822404 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-1d0b89fa78464881b04fbfc852393bf5 |
| Source note | uspto-grants-1989_04 |