HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 178527169, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 178527168 | HCID 178527168 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178527169 | HCID 178527169 | 65.1% |
Reaction Steps
To a stirred solution of 3.4 g of anhydrous piperazine in 25 ml of methanol is added 5.0 g of 3,7-dichloro-2H-1,2,4-benzothiadiazine 1,1-dioxide, while the mixture is cooled in an ice bath. After the addition, the mixture is stirred at room temperature for 3 hours. The crystalline precipitate is collected by suction filtration and treated with a mixture of 2 ml of concentrated hydrochloric acid and 40 ml of water. After removal of the insoluble materials by suction filtration, the filtrate is adjusted to a pH 8.0 with a dilute aqueous sodium hydroxide solution to give 3.9 g of the desired product, m.p. 292°-295° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04029780 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-80be55150e534c48a3e33d788bf89d65 |
| Source note | uspto-grants-1977_06 |