HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397666Generated: October 29, 2026
Hydrazinecarboxaldehyde → (2S)-1-[(4-fluorophenyl)sulfonyl]-2-(1H-1,2,4-triazol-3-yl)piperidine
https://huagongshe.com/reaction/397666
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazinecarboxaldehyde | HCID 12229 | — |
| Reactant | ethyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboximidate | HCID 57097015 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (2S)-1-[(4-fluorophenyl)sulfonyl]-2-(1H-1,2,4-triazol-3-yl)piperidine | HCID 178527361 | 32.6% |
Reaction Steps
Formylhydrazine (120 mg) was added to a solution of ethyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboximidate (295 mg) [see Preparation 41] in toluene (5 ml) and 1,4-dioxane (5 ml). The reaction mixture was stirred at reflux for 26 hours after which time the solvent was removed under reduced pressure. The residue was diluted with ethyl acetate and washed with water. The organic layer was separated, dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 100:0 changing to 0:100 (in 10% increments), by volume, hexane:ethyl acetate to afford (2S)-1-[(4-fluorophenyl)sulfonyl]-2-(1H-1,2,4-triazol-3-yl)piperidine (95 mg) as an off-white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610707B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-1c9e22cef2ba480d9c6bc29238cd09e3 |
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| Source note | uspto-grants-2003_08 |
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