HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714396Generated: October 29, 2026
HCID 44553783, compound → HCID 54746065, compound
https://huagongshe.com/reaction/714396
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 44553783 | HCID 44553783 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54746065 | HCID 54746065 | 50% |
Reaction Steps
A solution of N-benzyl-2-(4-(benzyloxy)-2-oxopyridin-1(2H)-yl)isonicotinamide (0.88 g, 2.14 mmol) and 20 weight % palladium on activated carbon (0.10 g) in methanol (50 mL) was stirred in atmospheric pressure of hydrogen for 2 hours. The resulting solution was filtered and concentrated in vacuo. The residue was recrystallized from methanol (10 mL) to give 4-hydroxy-2-oxo-2H-[1,2′]bipyridinyl-4′-carboxylic acid benzylamide as a colorless solid (0.34 g, 50%): mp 102-105° C. (methanol); 1H NMR (300 MHz, CD3OD) δ 8.66 (d, J=5.1 Hz, 1H), 8.05 (s, 1H), 7.81-7.78 (m, 2H), 7.36-7.24 (m, 5H), 6.20-6.17 (m, 1H), 5.86 (s, 1H) 4.57 (s, 2H); 13C NMR (75 MHz, CD3OD) δ 167.6, 164.0, 162.9, 150.8, 147.9, 142.4, 136.5, 135.9, 126.6, 125.7, 125.4, 119.5, 117.9, 100.9, 96.8, 41.8; MS (ES+) m/z 322.3 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187426B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-8452d365134a49fba0b54954406cc33e |
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| Source note | uspto-grants-2015_11 |
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