Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 86633491 | HCID 86633491 | — |
| Product | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 25233298 | HCID 25233298 | — |
Reaction Steps
To a solution of the title compound from Example 7 Step B (15.0 mg, 0.023 mmol) 1,4-dioxane (0.500 mL) was added lithium hydroxide (0.5 mL, 2.0 M in water, 1.00 mmol), and the resulting mixture was stirred at 50° C. After 30 min, the reaction mixture was rendered acidic by addition of aqueous hydrochloric acid, then was diluted with 1,4-dioxane and passed through a 0.45 micron syringe filter. Purification by reverse phase HPLC (30 to 100% acetonitrile in water, each with 0.1% v/v TFA) provided the title compound: LCMS m/z 614.2 [M+H]+; 1H NMR (500 MHz, d6-DMSO) δ 8.29 (s, 1H), 8.14 (d, J=8.0 Hz, 1H), 8.10 (t, J=8.0 Hz, 1H), 7.73 (dd, J=7.5, 1.5 Hz, 1H), 7.70 (d, J=8.0 Hz, 1H), 7.65 (d, J=8.5 Hz, 2H), 7.46-7.41 (m, 5H), 7.27 (d, J=8.5 Hz, 1H), 7.18 (d, J=8.5 Hz, 2H), 7.09 (t, J=7.5 Hz, 1H), 5.25 (s, 2H), 5.18 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455638B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-55f46761d1a14d999236e22f4e46ee56 |
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| Source note | uspto-grants-2013_06 |
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