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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386434Generated: October 30, 2026

5-(2-Pyridyl)oxazole → 1-Oxo-1-[5-(2-pyridyl)oxazol-2-yl]-3-(4-phenoxyphenyl)propane

https://huagongshe.com/reaction/386434

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-Pyridyl)oxazoleHCID 737194—
Reactant3-(4-Phenoxyphenyl)propanoic acidHCID 22036572—
Product1-Oxo-1-[5-(2-pyridyl)oxazol-2-yl]-3-(4-phenoxyphenyl)propaneHCID 1673516137%

Reaction Steps

The title compound (11f) was prepared from 5-(2-pyridyl)oxazole and 3-(4-phenoxyphenyl)propanoic acid (S30) using General Procedure B. PTLC (SiO2, 50% EtOAc-hexanes) afforded 11f (83 mg, 0.22 mmol, 37%) as a pale yellow solid: 1H NMR (CDCl3, 500 MHz) 8.69 (m, 1H), 7.89-7.86 (m, 2H), 7.82 (td, 1H, J=7.8, 1.8 Hz), 7.34-7.30 (m, 3H), 7.24 (d, 2H, J=8.5 Hz), 7.10-7.07 (m, 1H), 6.98 (d, 2H, J=12.1 Hz), 6.94 (d, 2H, J=8.6 Hz), 3.47 (t, 2H, J=7.4 Hz), 3.10 (t, 2H, J=7.4 Hz); 13C NMR (CDCl3, 100 MHz) 187.2, 157.4, 157.1, 155.5, 153.3, 150.1, 146.2, 137.1, 135.2, 129.7, 129.6, 126.9, 124.1, 123.0, 120.4, 119.1, 118.6, 40.7, 29.0; IR (film) νmax 3055, 2930, 1698, 1589, 1504, 1488, 1425, 1380, 1237, 1167, 1065, 871, 784, 692 cm−1; ESI-TOF m/z 371.1388 (C23H18N2O3+H+ requires 371.1396).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372823B2
Source datasetuspto-grants-2013_02
ORD IDord-0eb0c472e6fb4996acb2fe9824c6fe9d
Source noteuspto-grants-2013_02