HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252692Generated: October 26, 2026
Hydrochloric Acid → 1-Piperazinebutanamine, 4-(1,2-benzisothiazol-3-yl)-
https://huagongshe.com/reaction/1252692
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-[4-{4-(1,2-benzisothiazol-3-yl)-1-piperazinyl}butyl]phthalimide | HCID 10093606 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Piperazinebutanamine, 4-(1,2-benzisothiazol-3-yl)- | HCID 10565462 | — |
Reaction Steps
A mixture of N-[4-{4-(1,2-benzisothiazol-3-yl)-1-piperazinyl}butyl]phthalimide (1 g; 2.38 mmol), hydrazine hydrate (0.2 g; 3.57 mmol) and methanol (10 ml) was refluxed for 2.5 hours. After cooling, the reaction mixture was combined with a 10% aqueous hydrochloric acid solution (20 ml) and stirred. The precipitated crystals were removed by filtration, and the filtrate was neutralized with a 10% sodium hydroxide solution and extracted with chloroform. The organic layer was washed with a saturated sodium chloride solution and dried over magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by silica gel column chromatography to give the objective compound as an oily substance. IR νmaxfilm (cm-1): 3360, 3280, 3070, 1590, 1560, 1490.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04745117 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-a1c5a96f227c4464abd4d1b44211b5f3 |
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| Source note | uspto-grants-1988_05 |
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