HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → N-(5-Amino-1,2,4-triazol-3-yl)-2-nitrobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | methyl N-cyano-N'-(2-nitrophenyl)sulfonylcarbamimidothioate | HCID 178503935 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(5-Amino-1,2,4-triazol-3-yl)-2-nitrobenzenesulfonamide | HCID 13772880 | 82.2% |
Reaction Steps
A suspension of 29.4 g (98.0 mmol) of N'-Cyano-N-(2-nitrophenylsulfonyl)-S-methylisothiourea in 100 ml of acetonitrile was treated with 6.2 ml (6.3 g, 0.20 mol) of anhydrous hydrazine. A mild exothermic reaction occurred as the reaction mixture became homogeneous. After stirring for 9 days the precipitated solid was collected by filtration and dried to afford 22.9 g of yellow solid. The crude product was recrystallized from HOAc to yield a total of 15.9 g (57 percent) of the desired product as a pale yellow solid, mp 255°-256° C. IR and 1H NMR spectra were consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04638075 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-097c60612d5047d3bb1b7b2da28d485b |
| Source note | uspto-grants-1987_01 |