Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Pentafluorophenyl Trifluoroacetate | HCID 4327891 | — |
| Reactant | HCID 11392136 | HCID 11392136 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58962860 | HCID 58962860 | 82% |
Reaction Steps
4-(4-Ethyl-2-fluoro-phenylamino)-1-methyl-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (0.50 g, 1.72 mmol) was reacted with pentafluorophenyl trifluoroacetate (0.92 mL, 5.20 mmol) in the presence of pyridine (0.45 mL) in DMF (15 mL). The solution was allowed to stir at room temperature for 15 hours and then treated with 2-Amino-ethanol (0.50 mL, 8.60 mmol) as in example 75 to afford the 4-(4-Ethyl-2-fluoro-phenylamino)-1-methyl-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid (2-hydroxy-ethyl)-amide (0.47 g, 82%). 1H NMR [400 MHz, (CD3)2SO] δ 9.82 (s, 1H), 8.35 (t, J=5.4 Hz, 1H), 8.20 (s, 1H), 7.27 (t, J=8.4 Hz, 1H), 7.12 (d, J=11.8 Hz, 1H), 7.06 (d, J=7.7 Hz, 1H), 5.38 (s, 1H), 4.72 (t, J=5.1 Hz, 1 H, OH), 3.44 (t, J=11.5, 6.2 Hz, 2H), 3.35 (s, 3H), 3.22 (t, J=12.8, 6.8 Hz, 2H), 2.58 (q, J=7.1 Hz, 2H), 1.14 (t, J=7.1 Hz, 3H). (APCI+) calcd for C17H20FN3O3 333.36 (M+1), found 334.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07273877B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-c9702d1eb1714644bac50fd14fa0931e |
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| Source note | uspto-grants-2007_09 |
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