HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,1,3-Benzothiadiazole, 4-(1-piperazinyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 14581394 | HCID 14581394 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,1,3-Benzothiadiazole, 4-(1-piperazinyl)- | HCID 11424554 | — |
Reaction Steps
To a 50 ml round-bottomed flask equipped with condenser and N2 inlet were added 530 mg (1.83 mmol) 4-(2,1,3-benzothiadiazolyl)-N-vinyloxycarbonylpiperazine and 25 ml ethanol, and the suspension saturated with HCl gas. The reaction was refluxed 2.75 hours, cooled, and evaporated. The residue was triturated with acetone to give a yellow solid N-(2,1,3-benzothiadiazolyl)-piperazine, m.p. 240°-244° C., 365 mg (62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04883795 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-b55dcee954374a5c8a16289375858681 |
| Source note | uspto-grants-1989_11 |