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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178126Generated: November 3, 2026

HCID 66953970, compound → HCID 59559570, compound

https://huagongshe.com/reaction/1178126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66953970HCID 66953970—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59559570HCID 5955957043.1%

Reaction Steps

10% Pd/c (40 mg) was added to a stirred solution of 5-(3-benzyloxy-phenyl)-isoxazole-3-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amide (74 mg, 0.12 mmol) (prepared by the method as described above) in MeOH (30 mL) and stirred under hydrogen atmosphere. The reaction mixture was then stirred for 6 hrs. The mixture was filtered over a bed of celite. The celite was washed with MeOH and the filtrate was concentrated under reduced pressure to afford 26 mg (41.9% yield) of 5-(3-hydroxy-phenyl)-isoxazole-3-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amide. LCMS Purity: 99.07%. 1H NMR (CD3OD): δ 7.64 (m, 4H), 7.5 (d, 1H), 7.32 (m, 1H), 7.24 (s, 1H), 6.98 (m, 2H), 4.26 (m, 2H), 3.7 (m, 4H), 3.5 (m, 2H), 3.38 (m, 1H), 3.24 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-2c7dffda5098420b895b1e20cc950b05
Source noteuspto-grants-2010_11