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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205200Generated: November 1, 2026

N-bromobutanimide → 3-Bromo-6-chloro-2-methylimidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/2205200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant6-Chloro-2-methylimidazo(1,2-b)pyridazineHCID 10442072—
SolventChloroformHCID 6212—
Product3-Bromo-6-chloro-2-methylimidazo[1,2-b]pyridazineHCID 1371215490%

Reaction Steps

To a solution of 6-chloro-2-methylimidazo[1,2-b]pyridazine (2.00 g, 11.9 mmol, 1.0 equiv) in chloroform (50 mL) was added N-bromosuccinimide (2.55 g, 14.3 mmol, 1.2 equiv). The reaction was stirred at room temperature for 15 h. Purification by column chromatography using 50% ethyl acetate in hexanes elution gave 2.64 g of the yellow solid, 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09370515B2
Source datasetuspto-grants-2016_06
ORD IDord-640d062234ad42fa8b9b04a620e06e43
Source noteuspto-grants-2016_06