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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284627Generated: November 1, 2026

Bromoacetonitrile → HCID 86715536, compound

https://huagongshe.com/reaction/2284627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178484240HCID 178484240—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 86715536HCID 8671553653.5%

Reaction Steps

(E)-N′-(6-Bromopyridazin-3-yl)-N,N-dimethylformimidamide (2.5 g, 10.9 mmol), bromoacetonitrile (3.92 g, 32.7 mmol) and NaHCO3 (1.8 g, 21.8 mmol) in i-PrOH (15 mL) were heated at 75° C. for 8 h while stirring the contents. Subsequently, the dark reaction mixture was diluted with water and the resulting solid was collected by filtration. The solid was purified by flash chromatography (Combiflash® companion System® with RediSep® silica gel column 40 g and 15-30-50% EtOAC/hexanes as an eluting solvent) to obtain 1.3 g of 6-bromoimidazo[1,2-b]pyridazine-3-carbonitrile. 1H NMR (300 MHz, DMSO-d6) δ 8.58 (s, 1H), 8.33 (d, J=9.5 Hz, 1H), 7.77 (d, J=9.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145433B2
Source datasetuspto-grants-2015_09
ORD IDord-87e7f633f8ad421e9418254f49f4d91b
Source noteuspto-grants-2015_09