HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228485Generated: October 30, 2026
HCID 44434060, compound → HCID 59730173, compound
https://huagongshe.com/reaction/228485
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 44434060 | HCID 44434060 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59730173 | HCID 59730173 | 11.9% |
Reaction Steps
Combine 6-(2-Benzyl-2,3-dihydro-1H-isoindol-5-yloxy)-nicotinamide (230.0 mg, 0.67 mmol), EtOH (5 mL), 10% Pd—C (45.0 mg), and a Hydrogen balloon. Stir the reaction at room temperature for 168 hours at atmospheric pressure. Filter the reaction mixture through a pad of Celite using MeOH eluent and then concentrate the filtrate under reduced pressure. Add the mixture to a 2 g SCX column, wash with MeOH, and elute using 1N NH3-MeOH. After concentrating under reduced pressure, purify the mixture by flash chromatography using 10% 1N NH3-MeOH/DCM eluent to afford 19.2 mg, 0.08 mmol (11% yield) of the title compound as a white solid: 1H NMR (500 MHz, d-Methanol); 4.1-4.3 (4H, br m), 6.9-7.1 (3H, m), 7.3-7.4 (1H, m), 8.2-8.3 (1H, m), 8.6 (1H, s); MS m/z 254 (M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560463B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-884c93b1e8384b97ab4ce132a95b5643 |
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| Source note | uspto-grants-2009_07 |
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