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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269077Generated: November 1, 2026

N-bromobutanimide → HCID 18446605, compound

https://huagongshe.com/reaction/1269077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 18446628HCID 18446628—
SolventDichloromethaneHCID 6344—
ProductHCID 18446605HCID 1844660580%

Reaction Steps

To a solution of 7-chloro-2-(2-furyl)pyrazolo[1,5-a]pyridine-3-carbaldehyde (2.0 g, 8.06 mmol) in dichloromethane was added N-bromosuccinimide (2.01 g, 11.28 mmol). After stirring at room temperature for 2 hours, the reaction mixture was diluted with dichloromethane, washed with water and brine and dried over magnesium sulfate. Filtration and concentration followed by recrystallization with ethyl acetate gave 2-(5-bromo-2-furyl)-7-chloropyrazolo[1,5-a]pyridine-3-carbaldehyde (2.1 g, 80%) as a white solid. 1H NMR (CDCl3): δ 10.50 (s, 1H), 8.37 (dd, 1H), 7.47 (t, 1H), 7.20–7.18 (m, 2H), 6.54 (d, 1H). MS m/z 325 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199120B2
Source datasetuspto-grants-2007_04
ORD IDord-3e7db95745b4477f840bc10309f2dddd
Source noteuspto-grants-2007_04