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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389136Generated: October 29, 2026

Hydrazine hydrate (1:1) → HCID 58243744, compound

https://huagongshe.com/reaction/389136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 58244031HCID 58244031—
SolventAcetonitrileHCID 6342—
ProductHCID 58243744HCID 5824374479.2%

Reaction Steps

5-chloro-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl)-4H-1,2,4-triazol-3-yl}ethoxy)benzoic acid (1.00 g) was suspended in acetonitrile (10 ml), and WSC•monohydrochloride (654 mg) and HOBt (461 mg) were added to thereto, followed by stirring at room temperature for 30 minutes. A mixture of hydrazine monohydrate (1.1 ml) and acetonitrile (10 ml) was ice-cooled and the above reaction solution was added thereto, followed by stirring for 2 hours. The reaction solution was concentrated under reduced pressure and water and saturated aqueous sodium bicarbonate solution were added thereto, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (chloroform:methanol=100:1 to 99:5). The resulting solid was washed with diisopropylether to obtain, as a white solid, 5-chloro-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)benzohydrazide (817 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-47e0063363e14390b0c3f2c8123da0f2
Source noteuspto-grants-2013_02