HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093751Generated: October 29, 2026
HCID 178523508, compound → HCID 178523509, compound
https://huagongshe.com/reaction/1093751
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178523508 | HCID 178523508 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178523509 | HCID 178523509 | 35% |
Reaction Steps
10% Pd/C (50 mg) was added to a stirred solution of 5-(2-benzyloxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-oxo-2-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethyl}-amide (195 mg, 0.34 mmol) (prepared by method used for the synthesis of Intermediate 45) in methanol (30 mL) under inert atmosphere and stirred under H2 atmosphere with pressure for 3 hrs. The reaction mixture was filtered through celite, the celite was washed with methanol and the filtrate was concentrated under reduced pressure Washing with ethyl acetate afforded 58 mg (35% Yield) of 5-(2-hydroxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-oxo-2-[4-(3-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethyl}-amide. LC/MS [M+H]+: 489, 91.45%. 1H NMR (300 MHz, DMSO-d6): δ8.2 (m, 1H), 7.64 (d, 1H), 7.5 (t, 1H), 7.26 (t, 2H), 7.1 (m, 2H), 6.94 (m, 1H), 6.84 (t, 1H), 4.8 (m, 1H), 4.2 (d, 2H), 3.9 (m, 1H), 3.7 (m, 1H), 3.4 (m, 2H), 1.9 (m, 2H), 1.6 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129376B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-1abbc9f2b0c9481da16935630fc3101a |
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| Source note | uspto-grants-2012_03 |
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