HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178134Generated: November 2, 2026
HCID 178523553, compound → HCID 178523554, compound
https://huagongshe.com/reaction/1178134
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178523553 | HCID 178523553 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178523554 | HCID 178523554 | 46.2% |
Reaction Steps
10% Pd/c (25 mg) was added to a stirred solution of 5-(2-benzyloxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-[4-(5-fluoro-2-trifluoromethyl-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-amide (94 mg, 0.15 mmol) in a mixture of MeOH (60 mL) and THF (10 mL) and stirred under hydrogen atmosphere. The reaction mixture was then stirred for 1 hrs at room temperature. The mixture was filtered over a bed of celite. The celite was washed with MeOH and the filtrate was concentrated under reduced pressure. The crude was washed with ethyl acetate, filtered and dried to afford 36 mg (45% yield) of 5-(2-hydroxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-[4-(5-fluoro-2-trifluoromethyl-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-amide. LCMS Purity: 94.89%. 1H NMR (DMSO-d6): δ 13.2 (s, 1H), 10.4 (s, 1H), 7.9 (m, 2H), 7.5 (m, 2H), 6.9 (m, 3H), 4.1 (d, 2H), 3.4 (m, 6H), 3.1 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842696B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-48715484efe3437193488a80c917367b |
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| Source note | uspto-grants-2010_11 |
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