Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-(6-Bromo-4-chloroquinolin-3-yl)propan-1-one | HCID 86692845 | — |
| Reactant | HCID 178476567 | HCID 178476567 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178458755 | HCID 178458755 | 58% |
Reaction Steps
To a suspension of 1-(6-bromo-4-chloroquinolin-3-yl)propan-1-one (500 mg, 1.67 mmol) in dioxane (10 mL) and DMF (4 mL) was added trans-4-((dimethylamino)methyl)cyclohexanamine diacetic acid salt (583 mg, 2.11 mmol) and Cs2CO3 (3.27 g, 10.0 mmol). The resultant suspension was then heated to 90° C. and stirred for 5.5 h. The reaction mixture was cooled to room temperature and diluted with ethyl acetate. The solution was then washed with saturated sodium bicarbonate, water and then brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by column chromatography (silica, 0-10% methanol/dichloromethane) afforded the desired product (403 mg, 58%) as a tan solid. 1H NMR (300 MHz, CDCl3) δ 10.79 (d, J=8.4 Hz, 1H), 9.00 (s, 1H), 8.27 (d, J=2.0 Hz, 1H), 7.83-7.67 (m, 2H), 4.01-3.88 (m, 1H), 3.08 (q, J=7.2 Hz, 2H), 2.24 (s, 6H), 2.21-2.12 (m, 2H), 1.98 (d, J=13.4 Hz, 2H), 1.61-1.42 (m, 3H), 1.25 (t, J=7.3 Hz, 3H), 1.19-1.00 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120749B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-38e508ac79984bc19c7273a2743af9d3 |
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| Source note | uspto-grants-2015_09 |
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