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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968664Generated: October 29, 2026

N-bromobutanimide → HCID 85885309, compound

https://huagongshe.com/reaction/968664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant77493-88-0HCID 12726119—
SolventDichloromethaneHCID 6344—
ProductHCID 85885309HCID 8588530982%

Reaction Steps

7-Chloro-2-phenylpyrazolo[1,5-α]pyrimidine (0.1 g, 0.44 mmol, prepared as described in J. Med. Chem. 1981, 24, 610) was dissolved in dichloromethane (5 mL) and to this solution was added N-bromosuccinimide (108 mg, 0.61 mmol). The resulting reaction mixture was stirred for 30 minutes. Additional dichloromethane was added and the mixture was extracted with sodium hydroxide (1N), water and a saturated aqueous sodium chloride solution. The organic phase was dried over magnesium sulfate, filtered and concentrated. The resulting solid was purified by silica gel chromatography (ethyl acetate:hexane 1:2) to give 110 mg (82%) of 3-bromo-7-chloro-2-phenylpyrazolo[1,5-α]pyrimidine as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304068B2
Source datasetuspto-grants-2007_12
ORD IDord-dba069bb252d4b90971e273e29976acd
Source noteuspto-grants-2007_12