HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415294Generated: October 28, 2026
2-(3-(Pyridin-2-yl)phenyl)benzo[d]oxazole-7-carboxamide → 2-(3-(Piperidin-2-yl)phenyl)benzo[d]oxazole-7-carboxamide
https://huagongshe.com/reaction/415294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(3-(Pyridin-2-yl)phenyl)benzo[d]oxazole-7-carboxamide | HCID 66621185 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum dioxide monohydrate | HCID 11139377 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3-(Piperidin-2-yl)phenyl)benzo[d]oxazole-7-carboxamide | HCID 66621322 | 33.3% |
Reaction Steps
2-(3-(Pyridin-2-yl)phenyl)benzo[d]oxazole-7-carboxamide (90 mg, 0.28 mmol) and platinum (IV) oxide monohydrate (45 mg) in methanol (20 mL) was purged with 20 atm of hydrogen at 50° C. for 24 h. Then the mixture was filtered and adjusted to pH=9. The solvent was removed in vacuum. The crude was purified by chromatography (petroleum ether/ethyl acetate=1:1). 30 mg of 2-(3-(piperidin-2-yl)phenyl)benzo[d]oxazole-7-carboxamide was obtained, yield: 33%. 1H-NMR (400 MHz, DMSO-d6) δ 1.35-1.38 (m, 1H), 1.45-1.47 (m, 2H), 1.58-1.60 (m, 1H), 1.75-1.82 (m, 2H); 2.68-2.69 (m, 1H); 3.08-3.10 (d, J=9.6 Hz, 1H); 3.66-3.69 (m, 1H); 7.48-7.50 (t, J=6.0 Hz, 1H), 7.55-7.58 (d, J=6.4 Hz, 1H), 7.63-7.64 (d, J=5.6 Hz, 1H); 7.79-7.81 (m, 1H); 7.86 (brs, 1H); 7.94 (brs, 1H); 7.95-7.97 (m, 1H); 8.16-8.18 (m, 1H); 8.302 (s, 1H); LC-MS (ESI) m/z: 322 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088760B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-677d3a31801d4f779481a432a21482e1 |
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| Source note | uspto-grants-2012_01 |
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