HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269738Generated: October 30, 2026
Acetic Acid → 5-(4-benzyl-1-piperazinyl)-1H-indazole
https://huagongshe.com/reaction/1269738
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 69430818 | HCID 69430818 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(4-benzyl-1-piperazinyl)-1H-indazole | HCID 22933784 | 47.6% |
Reaction Steps
Acetic acid (2.6 ml) and water (0.7 ml) were added to a solution of 5-(4-benzyl-1-piperazinyl)-1-tetrahydro-2H-pyran-2-yl-1H-indazole (100 mg, 0.266 mmol) in tetrahydrofuran (1.3 ml) at room temperature and stirred 80° C. for 7 hours. Then, the reaction solution was concentrated and the resulting residue was diluted with ethyl acetate and washed with a saturated aqueous sodium hydrogencarbonate solution and then a saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent, and the resulting residue was purified by a thin-layer chromatography (eluent: chloroform/methanol=95/5) to obtain 5-(4-benzyl-1-piperazinyl)-1H-indazole (37 mg, 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07199147B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-637009381bcf4269a8a1c5a5a670423a |
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| Source note | uspto-grants-2007_04 |
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