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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910134Generated: October 30, 2026

4-Methylpyrazole → HCID 57743113, compound

https://huagongshe.com/reaction/910134

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpyrazoleHCID 3406—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantHCID 57743122HCID 57743122—
SolventDimethylformamideHCID 6228—
ProductHCID 57743113HCID 5774311371.2%

Reaction Steps

87 mg of sodium hydride (55% oil dispersion) was added to 3 ml of DMF, and to this was added a solution of 0.16 g of 4-methylpyrazole in 3 ml of DMF, and the mixture was stirred for 0.5 hours at room temperature. To the resultant mixture was added 0.25 g of 4-chloro-5-(4-chlorophenyl)-3,6-dimethylpyridazine, and the mixture was stirred for 3 hours on an oil bath of 80° C. To the reaction mixture was added ethyl acetate, and washed with brine four times. The organic layer was dried over anhydrous magnesium sulfate, then, concentrated under reduced pressure. 0.40 g of the resultant residue was subjected to silica gel column chromatography, to obtain 0.21 g of 5-(4-chlorophenyl)-3,6-dimethyl-4-(4-methyl-1-pyrazolyl)pyridazine (hereinafter, described as compound (5) of the present invention.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022073B2
Source datasetuspto-grants-2011_09
ORD IDord-dae0d567845c4db0be1ea8213613537d
Source noteuspto-grants-2011_09