Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 59520433 | HCID 59520433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11497604 | HCID 11497604 | — |
Reaction Steps
The crude (3-Chloro-4-{4-[2-(2,4-dichloro-phenoxy)-ethylcarbamoyl]-5-phenyl-isoxazol-3-yl}-phenyl)-acetic acid methyl ester 36 (0.85 mmol) is dissolved in THF (5 mL). A solution of 1 M LiOH in H2O (2 mL) is added and the mixture is stirred overnight at room temperature. The mixture is acidified with 1 M HCl (3 mL), DCM (50 mL) is added and the organic layer washed with H2O (3×30 mL). The organic layer is dried (MgSO4), filtered, concentrated and purified on reverse phase HPLC (H2O/MeCN gradient) to afford the title compound G1 as a white solid: 1H-NMR (400 MHz, CDCl3) δ=7.93 (dd, J=1.8 Hz, J=7.8 Hz, 2H), 7.52-7.23 (m, 7H), 7.17 (dd, J=8.8 Hz, J=2.5 Hz, 1H), 6.71 (d, J=8.8 Hz, 1H), 6.15 (t, J=5.3 Hz, NH), 3.92 (t, J=4.8 Hz, 2H), 3.72 (q, J=5.3 Hz, 2H), 3.50 (s, 2H). MS calculated for C26H20Cl3N2O5 (M+H+) 545.0, found 545.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820705B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-0112a59181d240e19b8306d7695f8cf7 |
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| Source note | uspto-grants-2010_10 |
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