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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429267Generated: October 26, 2026

Water → 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(2-imidazolin-2-yl)-4-trifluoromethylsulfinylpyrazole

https://huagongshe.com/reaction/429267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthylenediamineHCID 3301—
ReactantFipronilHCID 3352—
ReactantEthyl AcetateHCID 8857—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-(2-imidazolin-2-yl)-4-trifluoromethylsulfinylpyrazoleHCID 1835477238.4%

Reaction Steps

5-Amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfinyl-pyrazole (0.81 g, 1.85 mmol) was dissolved in 8 ml of THF, and then ethylenediamine (0.40 ml, 5.98 mmol) was added. The mixture was stirred at room temperature for 1 hour, heated to 50° C. and then stirred for 24 hours. Then, ethylenediamine (0.40 ml, 5.98 mmol) and THF (3 ml) were further added, followed by stirring for 14 hours. After the completion of the reaction, 20 ml of water was added and THF was distilled off and, further, 10 ml of water and 20 ml of an aqueous saturated sodium chloride solution were added. The mixture was extracted twice with 40 ml of ethyl acetate and the ethyl acetate layer was washed twice with 30 ml of an aqueous saturated sodium chloride solution. The resultant was dried over anhydrous magnesium sulfate and then concentrated to obtain a yellow amorphous. The amorphous was subjected to silica gel column chromatography [eluent: mixed solvent of ethyl acetate and hexane (volume ratio=1:2)] to obtain 0.34 g (0.71 mmol) of the title compound as a pale yellow amorphous. Yield 38%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316477B1
Source datasetuspto-grants-2001_11
ORD IDord-8e84db2929a445b39e3013327c589713
Source noteuspto-grants-2001_11