HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400331Generated: October 29, 2026
Acetic Anhydride → 1-(4-(4-bromo-1H-pyrazol-1-yl)piperidin-1-yl)ethanone
https://huagongshe.com/reaction/2400331
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-(4-bromo-1H-pyrazol-1-yl)piperidine hydrochloride | HCID 53407848 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1-(4-(4-bromo-1H-pyrazol-1-yl)piperidin-1-yl)ethanone | HCID 59392641 | 81.3% |
Reaction Steps
To a solution of 4-(4-bromopyrazol-1-yl)piperidine hydrochloride (300 mg, 1.13 mmol) in pyridine (3 ml) was added acetic anhydride (0.107 ml, 1.13 mmol) under an inert atmosphere. The reaction was stirred at 40° C., until reaction complete then evaporated under reduced pressure and re-evaporated with toluene twice, then partitioned between water and EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the product (250 mg), which was used without further purification MS: [M+H]+=272
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796244B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-4cc8b5081cb04140b2a1104b5bc99375 |
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| Source note | uspto-grants-2014_08 |
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