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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362898Generated: October 25, 2026

Acetohydrazide → 6-Chloro-3-methyl-(1,2,4)triazolo(4,3-b)pyridazine

https://huagongshe.com/reaction/1362898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydrazideHCID 14039—
Reactant3,6-DichloropyridazineHCID 67331—
Solvent1-ButanolHCID 263—
Product6-Chloro-3-methyl-(1,2,4)triazolo(4,3-b)pyridazineHCID 911387—

Reaction Steps

To a stirred solution of 1.0 g (6.7 mmol) of 3,6-dichloropyridazine in 5 mL of butanol was added 500 mg (6.7 mmol) of acetic hydrazide and the resulting solution was stirred under nitrogen at reflux for 24 h. The reaction mixture was then cooled to ambient temperature, filtered, and the resulting precipitate washed with ethyl acetate and methanol. The combined filtrate and washings were concentrated and dissolved in 250 mL of 10:1 chloroform/methanol then washed with saturated aqueous brine (2×100 mL). The organic phase was then dried over magnesium sulfate, filtered, and evaporated in vacuo to yield a yellow solid. The crude material was purified by flash chromatography on a Biotage Horizon® system (silica gel, 0 to 80% ethyl acetate/hexanes gradient) to give the title compound as a brown crystalline solid. LC/MS 169.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884104B2
Source datasetuspto-grants-2011_02
ORD IDord-4e9aaeeaf9014e7cb8f96aeb837a7ebd
Source noteuspto-grants-2011_02