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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726092Generated: November 1, 2026

Ammonium formate → 1-(5-hydroxy-1H-indazol-1-yl)-Ethanone

https://huagongshe.com/reaction/1726092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-(5-(Benzyloxy)-1H-indazol-1-yl)ethan-1-oneHCID 22567249—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(5-hydroxy-1H-indazol-1-yl)-EthanoneHCID 2256704860.5%

Reaction Steps

A suspension of 1 g of 1-(5-benzyloxyindazol-1-yl)ethanone, 1.42 g of ammonium formate and 0.59 g of palladium-on-charcoal at 10% in ethanol is refluxed for 16 hours. After returning to 20° C., the reaction mixture is filtered through a bed of celite and the filtrate is evaporated under reduced pressure. The crude compound thus obtained is triturated in 10 ml of diisopropyl ether and then filtered and dried under reduced pressure to obtain 400 mg of 1-(5-hydroxy-indazol-1-yl)-ethanone, which is characterized.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491710B2
Source datasetuspto-grants-2009_02
ORD IDord-5898f2d550ea46098ff5ee1536df1bff
Source noteuspto-grants-2009_02