Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 57855674 | HCID 57855674 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 25167324 | HCID 25167324 | 48.1% |
Reaction Steps
Pd/C (20 mg in 3 drops of water) was added to 4-(4-benzyloxy-phenoxy)-N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-benzamide (80 mg, 0.13 mmol) in MeOH (10 mL). The resulting reaction mixture was stirred at room temperature under an atmosphere of hydrogen for 3 hours. The reaction mixture was then filtered through a bed of celite. The methanol was removed to afford 80 mg of crude product. Purification by column chromatography (using silica gel of mesh size of 60-120 and 80/20 EtOAc:Hexane as the eluent) afforded 33 mg (48% yield) of 4-(4-hydroxy-phenoxy)-N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-benzamide LC-MS purity: 93%. 1H NMR (DMSO-D6): δ 9.4 (s, 1H), 8.5 (t, 1H), 7.9-7.5 (m, 6H), 6.8-7 (m, 5H), 4.2 (d, 2H), 3.5 (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-ddeb793f075e49d2833eeea870debed2 |
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| Source note | uspto-grants-2010_11 |
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