HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-3-(4-Benzyloxy-2,6-dichloro-benzyl)-1-(4,5,6,7-tetrahydro-1H-indazol-4-yl)-pyrrolidin-2-one → (R)-3-(2,6-Dichloro-4-hydroxy-benzyl)-1-(4,5,6,7-tetrahydro-1H-indazol-4-yl)-pyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-3-(4-Benzyloxy-2,6-dichloro-benzyl)-1-(4,5,6,7-tetrahydro-1H-indazol-4-yl)-pyrrolidin-2-one | HCID 67316437 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-3-(2,6-Dichloro-4-hydroxy-benzyl)-1-(4,5,6,7-tetrahydro-1H-indazol-4-yl)-pyrrolidin-2-one | HCID 67317194 | 87.2% |
Reaction Steps
To a solution of (R)-3-(4-benzyloxy-2,6-dichloro-benzyl)-1-(4,5,6,7-tetrahydro-1H-indazol-4-yl)-pyrrolidin-2-one (1.32 g) in ethanol (50 mL), add palladium hydroxide on carbon (10%, 0.65 g). Stir the mixture under hydrogenation (50 psi) at room temperature for 3 hours. Filter the mixture through celite. Remove the solvent in vacuo to afford 0.93 g of the title compound. MS (m/z): 380 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981918B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-c418ae8aa8cd4db1b1e8297e494bdd47 |
| Source note | uspto-grants-2011_07 |