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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217692Generated: October 26, 2026

Cyanogen Bromide → 6-Chloro-8-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromide

https://huagongshe.com/reaction/217692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant6-Chloro-3-hydrazinyl-4-methylpyridazineHCID 11446490—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Chloro-8-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromideHCID 86650796—

Reaction Steps

(6-Chloro-4-methylpyridazin-3-yl)hydrazine (W3.002; 4.6 g) were initially charged in EtOH (330 ml) and water (70 ml) while stirring at RT. Thereafter, cyanogen bromide in a mixture of EtOH (170 ml) and water (30 ml) was slowly added dropwise at RT. After stirring at RT for 6 h, the mixture was left to stand overnight. Then the mixture was dried and the residue was purified using silica gel (40 g cartridge, DCM/methanol gradient of 0-10% in 30 min). 7.3 g of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-b4614576bfab4dd4b2399c21f7253d21
Source noteuspto-grants-2012_06