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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178136Generated: October 30, 2026

HCID 178523540, compound → HCID 178523541, compound

https://huagongshe.com/reaction/1178136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178523540HCID 178523540—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178523541HCID 17852354142%

Reaction Steps

10% Pd/c (20 mg) was added to a stirred solution of 5-(2-Benzyloxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amide (103 mg, 0.17 mmol))(prepared by the method as described above) in MeOH (50 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 35.8 mg (41.3% yield) of 5-(2-Hydroxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-amide. LCMS Purity: 93.92%. 1H NMR (DMSO): δ 13.1 (s, 1H), 10.3 (s, 1H), 8.2 (s, 1H), 7.74 (m, 2H), 7.62 (m, 2H), 7.52 (m, 1H), 7.16 (m, 1H), 7.04 (s, 1H), 6.96 (m, 1H), 6.86 (m, 1H), 4.1 (m, 2H), 3.55 (m, 4H), 3.4 (m, 2H), 3.2 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-a3657be2165b4a7aa369b66d34730093
Source noteuspto-grants-2010_11