HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-((4-(4-Cyclopropylpiperazin-1-yl)piperidin-4-yl)methyl)isoindolin-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-((1-Benzyl-4-(4-cyclopropylpiperazin-1-yl)-piperidin-4-yl)methyl)isoindolin-1-one | HCID 57989590 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-((4-(4-Cyclopropylpiperazin-1-yl)piperidin-4-yl)methyl)isoindolin-1-one | HCID 57436815 | 60% |
Reaction Steps
Through a solution of 2-((1-Benzyl-4-(4-cyclopropylpiperazin-1-yl)-piperidin-4-yl)methyl)isoindolin-1-one (0.63 mmol) in ethanol (10 ml) was passed argon gas for 10 min. Then acetic acid (200 μl) and Pd(OH)2 (20% by weight) were added to the reaction mixture. The mixture was stirred at room temperature for 16 h under an atmosphere of H2 by using a hydrogen balloon. The reaction mixture was filtered through celite and the filtrate was concentrated to dryness to give the desired product. Yield: 60%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541573B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-4653a2898c2340348b1372a46ce7c63b |
| Source note | uspto-grants-2013_09 |