Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 131735024 | HCID 131735024 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 131735028 | HCID 131735028 | — |
Reaction Steps
To a solution of (3-benzyl-4-chloro-2-methoxyquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)(6-(trifluoromethyl)pyridin-3-yl)methanol (446 mg, 0.830 mmol, Example 110) and DMF (15 mL) was added NaH (60% in mineral oil, 90 mg, 2.3 mmol) at room temperature. After stirring for 15 minutes, acetic anhydride (0.16 mL, 1.7 mmol) was added. After stirring for 1 hour, NH3 (7.0 M in MeOH, 1.0 mL, 7.0 mmol) was added. The mixture was stirred overnight and concentrated in vacuo. The residue was partitioned between EtOAc and water. The organic layers were washed with water, and the aqueous layer was back extracted with EtOAc. The extracts were dried (Na2SO4), filtered, and concentrated. The residue was purified by reverse phase HPLC (water/acetonitrile/0.1% TFA) to afford the title compound as a TFA salt. 1H NMR (400 MHz, MeOH-d4) δ 8.97 (s, 1H), 8.77 (d, J=2.02 Hz, 1H), 8.11 (d, J=2.02 Hz, 1H), 8.00 (dd, J=2.27, 8.34 Hz, 1H), 7.94 (d, J=9.09 Hz, 1H), 7.88 (d, J=8.08 Hz, 1H), 7.62 (dd, J=2.27, 8.84 Hz, 1H), 7.20-7.24 (m, 4H), 7.12-7.18 (m, 1H), 6.94 (d, J=1.52 Hz, 1H), 4.30 (s, 2H), 4.08 (s, 3H), 3.72 (s, 3H); MS m/e 538.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284308B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-07bb05c48992495785cd772b353a3688 |
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| Source note | uspto-grants-2016_03 |
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