Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | 2,5-Dichloro-4-iodopyridine | HCID 53400965 | — |
| Reactant | HCID 67075766 | HCID 67075766 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86655136 | HCID 86655136 | 48% |
Reaction Steps
2,5-Dichloro-4-iodopyridine (0.2 g, 0.73 mmol), 6-amino-4-methyl-2,3-dihydro-1,4-benzoxazepin-5-one (0.140 g, 0.73 mmol), palladium(II) acetate (6.56 mg, 0.03 mmol), 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (0.025 g, 0.04 mmol) and cesium carbonate (0.476 g, 1.46 mmol) were suspended in dioxane (5 mL). The mixture was heated at 100° C. for 30 minutes in a microwave reactor and then allowed to cool to room temperature. The mixture was loaded onto an SCX column and the product eluted first with MeOH and then with a 7M solution of NH3 in MeOH. Fractions containing product were combined and evaporated. The residue was purified by chromatography on silica, eluting with a gradient of 0-5% MeOH in CH2Cl2. Fractions containing product were combined and evaporated to afford 6-[(2,5-dichloropyridin-4-yl)amino]-4-methyl-2,3-dihydro-1,4-benzoxazepin-5-one (0.118 g, 48% yield); 1H NMR spectrum: (300 MHz, DMSO) δ 3.10 (3H, s), 3.55 (2H, t), 4.34 (2H, t), 6.88-6.91 (1H, m), 7.13 (1H, s), 7.36-7.39 (1H, m), 7.50 (1H, t), 8.26 (1H, s), 9.31 (1H, s); Mass spectrum: m/z (ESI+) (M+H)+ =337.96 and 339.99 and 341.96.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569298B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-f6bd6027626f4c44bbca6539bf01eaac |
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| Source note | uspto-grants-2013_10 |
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