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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993916Generated: October 31, 2026

N-bromobutanimide → HCID 68678536, compound

https://huagongshe.com/reaction/1993916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 68677540HCID 68677540—
SolventDichloromethaneHCID 6344—
SolventAluminumHCID 5359268—
ProductHCID 68678536HCID 6867853652.2%

Reaction Steps

To a solution of 1-phenyl-4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyridin-2-one (0.21 g) in methylene chloride (4 mL) was added N-bromosuccinimide (0.18 g). The reaction vessel was wrapped in aluminium foil and stirred for 24 hours. The solvent was evaporated in vacuo and the residue was dissolved in EtOAc and water. The phases were separated and the aqueous phase was extracted with more EtOAc. The combined organic phases were washed with brine, dried over sodium sulfate, filtered and reduced in vacuo to give a crude residue. Flash column chromatography over silica gel using ISCO combiflash chromatography and eluting with EtOAc/heptane afforded the desired 3-bromo-1-phenyl-4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyridin-2-one (0.15 g) as a light brown solid. MS (ESI+): 295.2 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652057B2
Source datasetuspto-grants-2010_01
ORD IDord-4bfd2bea6302467aab21b3a978edbaaa
Source noteuspto-grants-2010_01