HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437121Generated: October 29, 2026
1-Methylpiperazine → HCID 178480777, compound
https://huagongshe.com/reaction/437121
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 178526645 | HCID 178526645 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178480777 | HCID 178480777 | 27.3% |
Reaction Steps
To a stirred suspension of 1.0 g of 3-(m-nitrobenzenesulfonyloxy)-2H-1,2,4-benzothiadiazine 1,1-dioxide in 10 ml of acetone is added dropwise 0.53 g of 1-methylpiperazine, while the mixture is cooled in an ice bath. After the addition, the mixture is stirred at room temperature for 1 hour. After removal of acetone by distillation under reduced pressure, 30 ml of water is added to the residue. The crystalline precipitate is collected by suction filtration and treated with 2 ml of a 10% aqueous sodium hydroxide solution. After removal of the insoluble materials by suction filtration, the filtrate is adjusted to a pH 8.0 with dilute hydrochloric acid. The crystalline precipitate is collected by suction filtration and recrystallized from a mixture of dimethylformamide and water to give 0.2 g of the desired product, m.p. 265°-267° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04029780 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-a626a82bc33141628f33c8ff0e05b8aa |
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| Source note | uspto-grants-1977_06 |
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