HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 1-(5-hydroxy-1H-indazol-1-yl)-Ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 1-(5-(Benzyloxy)-1H-indazol-1-yl)ethan-1-one | HCID 22567249 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(5-hydroxy-1H-indazol-1-yl)-Ethanone | HCID 22567048 | 60.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07491710B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-5898f2d550ea46098ff5ee1536df1bff |
| Source note | uspto-grants-2009_02 |