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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062781Generated: November 3, 2026

Acetic Acid → N-[4-(1-methylethoxy)phenyl]-1H-pyrazol-5-amine

https://huagongshe.com/reaction/2062781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium formateHCID 2723923—
Reactant1-benzyl-N-[4-(1-methylethoxy)phenyl]-1H-pyrazol-5-amineHCID 67009800—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductN-[4-(1-methylethoxy)phenyl]-1H-pyrazol-5-amineHCID 6700938866%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 1-benzyl-N-[4-(1-methylethoxy)phenyl]-1H-pyrazol-5-amine (0.80 g) and palladium hydroxide (10 wt %, 0.80 g) in ethanol (4.5 mL)-acetic acid (0.5 mL) was added ammonium formate (0.49 g) at 80° C. After stirring at 80° C. for 2 hr, the mixture was allowed to cool, ethyl acetate was added, and the insoluble material was filtered off. Saturated aqueous sodium hydrogen carbonate solution was added to the filtrate, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography to give the title compound as a pale-yellow amorphous solid (0.37 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283353B2
Source datasetuspto-grants-2012_10
ORD IDord-bff9371da4c94fb0aa684f2549216b3d
Source noteuspto-grants-2012_10