Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 68869663 | HCID 68869663 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10196028 | HCID 10196028 | — |
Reaction Steps
A solution of 2-Ethoxy-2-methyl-3-(4-{2-[3-methyl-2-oxo-1-(4-trifluoromethyl-benzyl)-imidazolidin-4-yl]-ethoxy}-phenyl)-propionic acid ethyl ester (0.19 g, 0.347 mmol) and 5N NaOH (0.5 mL) in ethanol (5 mL) is refluxed for 1 h, cooled to ambient temperature, and concentrated. The residue is diluted with CH2Cl2, washed, dried, and concentrated in vacuo to provide the title compound. 1H NMR (400 MHz, CDCl3): δ 7.63 (d, 2H, J=8.4 Hz), 7.44 (d, 2H, J=8.4 Hz), 7.08 (d, 2H, J=8.7 Hz), 6.76 (d, 2H, J=8.7 Hz), 4.37, 4.35 (ABq, 2H, J=16.4 Hz), 3.99-3.89 (m, 2H), 3.63-3.53 (m, 1H), 3.43-3.23 (m, 2H), 2.98 (t, 1H, J=8.8 Hz), 2.86, 2.84 (ABq, 2H, J=15.4 Hz), 2.71 (s, 3H), 2.51-2.49 (m, 3H), 2.23-2.13 (m, 1H), 1.86-1.74 (m, 1H), 1.15 (s, 3H), 1.08 (t, 3H, J=6.9 Hz). MS [ES+] m/z exact mass calcd for C26H32N2O5F3 509.2263, found 509.2288.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544812B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-1f0ebde1fced4ddd9b3bbece79b5c469 |
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| Source note | uspto-grants-2009_06 |
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