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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217695Generated: October 31, 2026

Cyanogen Bromide → HCID 58136812, compound

https://huagongshe.com/reaction/217695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86650805HCID 86650805—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventWater ethanolHCID 19096565—
ProductHCID 58136812HCID 58136812—

Reaction Steps

(6-Chloro-4-isopropylpyridazin-3-yl)hydrazine trifluoroacetic acid salt (W3.009; 258 mg) was initially charged in ethanol/water (6/1 ml) at RT while stirring. Thereafter, cyanogen bromide (182 mg, dissolved in a mixture of 1.5 ml of EtOH and 0.5 ml of water) was cautiously added dropwise. After stirring for 5 hours, the mixture was left to stand overnight, another 1 eq. of the cyanogen bromide solution was added and the mixture was stirred all day. After standing overnight, the solvent was drawn off and the residue was admixed with water. Once the residue had been alkalized with saturated potassium carbonate solution, it was extracted three times with dichloromethane. The combined organic phases were dried over sodium sulfate and, after filtering off the desiccant, dried under reduced pressure. 180 mg of the title compound were obtained in sufficient purity. LC-MS rt: 0.65 min [M+H]+: 212.1 (met. b)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-ca23f20fdba34cebaa788a5cd2a49994
Source noteuspto-grants-2012_06