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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396945Generated: November 1, 2026

HCID 178444619, compound → HCID 178444621, compound

https://huagongshe.com/reaction/1396945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178444619HCID 178444619—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductHCID 178444621HCID 17844462173.5%

Reaction Steps

To a 50 mL round-bottomed flask was added (3S)-3-{[(5-fluoro-1-oxido-2-pyridinyl)amino]carbonyl}-2-[(2R)-2-({formyl[(phenylmethyl)oxy]amino}methyl)heptanoyl]-1-pyrazolidinecarboxylate (103 mg, 0.162 mmol) in methanol (3 ml), followed by Pearlman's catalyst (10 mg). The mixture was stirred under a balloon of H2 for 37 min, and the catalyst was filtered off. The filtrate was concentrated and the residue was purified by RP-HPLC to provide (3S)—N-(5-fluoro-1-oxido-2-pyridinyl)-2-((2R)-2-{[formyl(hydroxy)amino]methyl}heptanoyl)-3-pyrazolidinecarboxamide (49 mg, 73%). LCMS: (M+H)+: 412.0. 1H NMR (400 MHz, METHANOL-d4) δ ppm 0.76-0.98 (m, 3H) 1.26-1.46 (m, 6H) 1.48-1.57 (m, 1H) 1.63-1.77 (m, 1H) 2.30-2.44 (m, 1H) 2.46-2.59 (m, 1H) 2.91 (td, J=10.67, 6.44 Hz, 1H) 3.20-3.29 (m, 1H) 3.52 (dd, J=13.77, 4.42 Hz, 1H) 3.77-3.96 (m, 2H) 4.81-4.88 (m, 1H) 7.47 (ddd, J=9.66, 7.14, 2.65 Hz, 1H) 7.90 (s, 1H) 8.40-8.61 (m, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-78d61e3ddf534102ada36dfb849c54b2
Source noteuspto-grants-2014_12