HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499609Generated: November 1, 2026
HCID 86726828, compound → HCID 86726827, compound
https://huagongshe.com/reaction/1499609
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86726828 | HCID 86726828 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86726827 | HCID 86726827 | 100% |
Reaction Steps
A solution of 4-{(3R,4R,5S)-4-(acetyloxy)-3-[(tert-butoxycarbonyl)amino]-5-cyclopropylpiperidin-1-yl}-3-nitro-6,7-dihydro-5H-cyclopenta[b]pyridin-7-yl acetate (0.055 g, 0.11 mmol) in MeOH (5.0 mL) and EtOAc (1.0 mL) was deoxygenated and purged with nitrogen prior to the addition of 10% palladium (dry basis) on activated carbon (wet, Degussa type E101 NE/W) (0.025 g). The reaction mixture was stirred under an atmosphere of hydrogen, introduced via a balloon, for 2 h. The crude reaction mixture was filtered through a pad of diatomaceous earth and the solids were washed thoroughly with EtOAc and MeOH. The filtrate was concentrated under reduced pressure to afford the sub-title compound (0.052 g, 100%). LCMS (ESI) m/z calc. for C25H37N4O6 489.3 [M+H]+. found 489.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09200004B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-d17f9ad824d040b09ad19641fe7bb15c |
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| Source note | uspto-grants-2015_12 |
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