HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093673Generated: October 30, 2026
HCID 57874431, compound → HCID 57874485, compound
https://huagongshe.com/reaction/1093673
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57874431 | HCID 57874431 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57874485 | HCID 57874485 | 30.6% |
Reaction Steps
To a solution of N-biphenyl-4-yl-3-[4-(2-nitro-phenoxy)-piperidin-1-yl]-3-oxo-propionamide (0.09 g, 0.00019 mole) in methanol (10 mL) was added 10% Pd/C (0.015 g) and the resulting mixture was stirred under an atmosphere of hydrogen for 30 minutes. The mixture was then filtered through celite, the celite was washed with methanol and the organic layers were concentrated under reduced pressure. The resulting residue was recrystallized from a mixture of hexane and chloroform to afford 0.025 g (29%) of 3-[4-(2-amino-phenoxy)-piperidin-1-yl]-N-biphenyl-4-yl-3-oxo-propionamide. LC-MS purity: 430.21 (M+1)+, 90.7%, 1H NMR (DMSO-d6): δ 7.7 (m, 6H), 7.4 (m, 2H), 7.3 (m, 1H), 6.8 (m, 1H), 6.6 (m, 2H), 6.5 (m, 1H), 4.6 (bs, 2H), 4.5 (bs, 1H), 3.8 (m, 2H), 3.5 (m, 4H), 2.0 (m, 2H), 1.8 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129376B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-3ef06eb8a4b84800a24efaefc0fb5cc5 |
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| Source note | uspto-grants-2012_03 |
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