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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217676Generated: October 29, 2026

Cyanogen Bromide → HCID 58136866, compound

https://huagongshe.com/reaction/217676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 53434476HCID 53434476—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 58136866HCID 58136866—

Reaction Steps

(6-Ethylpyridazin-3-yl)hydrazine hydrochloride (2 g) was initially charged in a mixture of ethanol (30 ml) and water (6 ml) while stirring at RT. Thereafter, cyanogen bromide was cautiously added dropwise (2.4 g dissolved in 7.5 ml of ethanol and 1.5 ml of water). After stirring at RT for one hour, the mixture was left to stand overnight and, the next day, stirred for 4 further hours. The solvent was then drawn off and the residue was purified by means of preparative HPLC (met. C). The clean product fractions were combined, freed of the acetonitrile under reduced pressure, alkalized with saturated potassium carbonate solution and extracted repeatedly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated. 830 mg of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-7f233e7fcd074eedb5e310115c80a6af
Source noteuspto-grants-2012_06