Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86731755 | HCID 86731755 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86731754 | HCID 86731754 | — |
Reaction Steps
To a solution of 5-amino-3-[(4,6-dimethylpyridin-2-yl)amino]pyridine-2-carboxamide TFA salt (50 mg, 0.13 mmol) in THF (1 mL) was added ethyl isocyanate (12 mg, 0.18 mmol) and triethylamine (0.075 mL, 0.54 mmol), and the reaction mixture was stirred for 2 hours at room temperature. Additional ethyl isocyanate (12 mg, 0.18 mmol) and triethylamine (0.075 mL, 0.54 mmol) were added, and the reaction mixture was heated to 55° C. for 18 hours. The reaction mixture was allowed to cool to room temperature and concentrated under reduced pressure. The residue was purified by reverse phase HPLC (acetonitrile/water with 0.1% TFA, linear gradient) to afford 3-[(4,6-dimethylpyridin-2-yl)amino]-5-[(ethylcarbamoyl)amino]pyridine-2-carboxamide. MS ESI calc'd. for C16H21N6O2 [M+H]+ 329. found 329. 1H NMR (500 MHz, DMSO-d6) δ 11.61 (s, 1H), 9.24 (s, 1H), 8.86 (s, 1H), 8.23 (d, J=2.2 Hz, 1H), 8.13 (s, 1H), 7.57 (s, 1H), 6.63 (s, 1H), 6.53 (s, 1H), 6.33 (t, J=5.3 Hz, 1H), 3.20-3.07 (m, 2H), 2.40 (s, 3H), 2.23 (s, 3H), 1.06 (t, J=7.2 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216173B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-58c4e83bef2546caa50e73f7b277de90 |
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| Source note | uspto-grants-2015_12 |
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