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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742062Generated: November 2, 2026

Triethylamine → 5-Amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazole

https://huagongshe.com/reaction/1742062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
Reactantalpha-Chloro-3-nitrobenzaldoximeHCID 2756318—
Solvent1,4-DioxaneHCID 31275—
Product5-Amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazoleHCID 7350841675%

Reaction Steps

4.85 g (0.05 mol) of 3(5)-amino-5(3)-methyl-pyrazole in 50 ml of absolute dioxan are treated with 8.3 ml (0,06 mol) of triethylamine and then, under stirring at room temperature, are treated dropwise with a solution of 10 g (0.05 mol) of 3-nitro-benzohydroximoyl chloride in 50 ml of absolute dioxan. Stirring is continued for 3 hours and then the mixture is evaporated to dryness. The residue is treated with water and ethyl acetate. The organic phase is dried over magnesium sulphate, evaporated under vacuum and the residue obtained in this way is recrystallised from dioxan. 9.8 g (48%) of 5-amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazole with a m. pt. of 224° to 226° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05336780
Source datasetuspto-grants-1994_08
ORD IDord-9951e2f903c54e1da04e592485a75fc4
Source noteuspto-grants-1994_08