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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429317Generated: October 25, 2026

(3-Methoxyphenyl)hydrazine → {1-(3-Methoxyphenyl)-5-[4-(methylthio)-phenyl]pyrazol-3-yl}amine

https://huagongshe.com/reaction/429317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Methoxyphenyl)hydrazineHCID 423605—
Reactant3-[4-(Methylthio)phenyl]acrylonitrileHCID 4239680—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product{1-(3-Methoxyphenyl)-5-[4-(methylthio)-phenyl]pyrazol-3-yl}amineHCID 1835540251.3%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a mixture of (3-methoxyphenyl)hydrazine (6 g) and 3-[4-(methylthio)phenyl]acrylonitrile (5.7 g) in methanol (100 ml) was added sodium methoxide (28 wt. % solution in methanol) (18 ml) at ambient temperature. The mixture was heated to dryness under nitrogen at 140° C. for 30 minutes. The resultant orange mass was partitioned between dichloromethane and ice water. The organic layer was dried over magnesium sulfate, and then filtered. This filtrate was evaporated in vacuo. The resultant mass was dissolved in ethyl acetate (150 ml) and refluxed for 1 hour in the presence of magnesium (IV) oxide (20 g). This mixture was cooled, and filtered. The filtrate was evaporated in vacuo. The resultant mass was purified by column chromatography on silica gel using dichloromethane as eluent to give {1-(3-methoxyphenyl)-5-[4-(methylthio)-phenyl]pyrazol-3-yl}amine (5.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316485B1
Source datasetuspto-grants-2001_11
ORD IDord-41084b0c456a40eaa0dae9ac6d0370c3
Source noteuspto-grants-2001_11