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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217697Generated: October 28, 2026

Cyanogen Bromide → HCID 58136913, compound

https://huagongshe.com/reaction/217697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86650808HCID 86650808—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventWater ethanolHCID 19096565—
ProductHCID 58136913HCID 58136913—

Reaction Steps

(6-Chloro-5-isopropylpyridazin-3-yl)hydrazine trifluoroacetic acid salt (W3.013; 400 mg) was initially charged in ethanol/water (6/1 ml) at RT while stirring. Thereafter, cyanogen bromide (353 mg, dissolved in a mixture of 1 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 and stirred for a further 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. 400 mg of the title compound were obtained in sufficient purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-4b6d075309c942d48e7d5b99f13bb4a8
Source noteuspto-grants-2012_06