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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396986Generated: November 1, 2026

(3R)-3-(cyclopentyl methyl)-4-[(5S)-5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxo-N-[(phenylmethyl)oxy]butanamide → (3R)-3-(cyclopentylmethyl)-N-hydroxy-4-[(5S)-5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxobutanamide

https://huagongshe.com/reaction/1396986

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R)-3-(cyclopentyl methyl)-4-[(5S)-5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxo-N-[(phenylmethyl)oxy]butanamideHCID 86706403—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product(3R)-3-(cyclopentylmethyl)-N-hydroxy-4-[(5S)-5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxobutanamideHCID 8670640439.2%

Reaction Steps

To a solution of (3R)-3-(cyclopentylmethyl)-4-[(5S)-5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxo-N-[(phenylmethyl)oxy]butanamide (57 mg, 0.12 mmol) in methanol (5 mL) was added Pearlman's catalyst (17 mg, 0.024 mmol). The mixture then was stirred under 1 atm of H2 for 1 hour. After 1 hour, the mixture was filtered, concentrated, and purified by Gilson HPLC (Sunfire Column 19×50 mm, flowrate 25 mL/min, 10 min, 5-65% MeCN:H2O) to afford (3R)-3-(cyclopentylmethyl)-N-hydroxy-4-[(5S)-5-(4-morpholinylcarbonyl)-4,5-dihydro-1H-pyrazol-1-yl]-4-oxobutanamide (19 mg, 0.047 mmol, 39% yield) as a white solid. MS: 381 ([M+H]+). 1H NMR (400 MHz, METHANOL-d4) δ ppm 1.07-1.29 (m, 2H) 1.36-1.48 (m, 1H) 1.50-1.69 (m, 4H) 1.72-2.03 (m, 5H) 2.19-2.30 (m, 1H) 2.36-2.53 (m, 1H) 2.77-3.01 (m, 2H) 3.46-3.98 (m, 10H) 5.15-5.29 (m, 1H) 7.03-7.07 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-94a6042cd51048dc9fbdc3ff3198f7f0
Source noteuspto-grants-2014_12