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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-(4-bromo-1H-pyrazol-1-yl)piperidine hydrochlorideHCID 53407848—
SolventPyridineHCID 1049—
Product1-(4-(4-bromo-1H-pyrazol-1-yl)piperidin-1-yl)ethanoneHCID 5939264181.3%

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796244B2
Source datasetuspto-grants-2014_08
ORD IDord-4cc8b5081cb04140b2a1104b5bc99375
Source noteuspto-grants-2014_08