HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402852Generated: October 30, 2026
HCID 57722465, compound → HCID 57722467, compound
https://huagongshe.com/reaction/402852
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 57722465 | HCID 57722465 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57722467 | HCID 57722467 | 87% |
Reaction Steps
2-{(3R,6R)-3-(2,3-Dihydro-1H-inden-2-yl)-6-[(1S)-1-methylpropyl]-2,5-dioxo-1-piperazinyl}-2-(4,6-dimethyl-3-pyridinyl)-N-{2-[(phenylmethyl)oxy]phenyl}acetamide (intermediate 3) (3.30 g) was dissolved in ethanol (75 ml) and hydrogenated over palladium on charcoal (wet 10% Pd, 0.50 g) for 20 hours. The catalyst was removed by filtration and washed with dichloromethane. The combined filtrate and washings were evaporated in vacuo. The residue was applied to a 90 g Biotage column and eluted with ethyl acetate. The required fractions were combined and evaporated in vacuo to give 2-{(3R,6R)-3-(2,3-dihydro-1H-inden-2-yl)-6-[(1S)-1-methylpropyl]-2,5-dioxo-1-piperazinyl}-2-(4,6-dimethyl-3-pyridinyl)-N-(2-hydroxyphenyl)acetamide (2.43 g, 87%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742099B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-de94ebc85f2446fa9a655366fa677470 |
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| Source note | uspto-grants-2014_06 |
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