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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-(Pyridin-2-yl)phenyl)benzo[d]oxazole-7-carboxamideHCID 66621185—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum dioxide monohydrateHCID 11139377—
SolventMethanolHCID 887—
Product2-(3-(Piperidin-2-yl)phenyl)benzo[d]oxazole-7-carboxamideHCID 6662132233.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-677d3a31801d4f779481a432a21482e1
Source noteuspto-grants-2012_01