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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635511Generated: October 30, 2026

m-Tolylhydrazinium(1+) chloride → 2-chloro-4-[1-(3-methylphenyl)-3-methyl-1H-pyrazol-5-yl]pyridine

https://huagongshe.com/reaction/1635511

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Tolylhydrazinium(1+) chlorideHCID 71562—
ReactantAmmonia hydroxideHCID 21862953—
ReactantHCID 53955776HCID 53955776—
SolventEthanolHCID 702—
Product2-chloro-4-[1-(3-methylphenyl)-3-methyl-1H-pyrazol-5-yl]pyridineHCID 1148298387%

Reaction Steps

To a mixture of 1-(2-chloroisonicotinyl)-1,3-butanedione (1.35 g, 0.068 mol) and 3-methylphenylhydrazine hydrochloride (1.30 g, 0.0082 mol) in ethanol (40 mL) was added ammonia hydroxide (0.96 mL, 0.0082 mol) dropwise. The reaction mixture was heated at reflux overnight. The solvent was removed and the residue was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated and the crude was purified by chromatography on silica gel (ethyl acetate/hexane, 2:8) to give 1.68 g (87% yield) of product as a yellow oil: Anal. Calcd. for C16H14ClN3: C, 67.72; H, 4.97; N, 14.81; Cl, 12.49. Found: C, 67.91; H, 5.08; N, 14.79; Cl, 12.40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509361B1
Source datasetuspto-grants-2003_01
ORD IDord-4b07217005f644799ac1019134ab52a2
Source noteuspto-grants-2003_01