Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | 2-Amino-6-methylpyridine-3-carboxylic acid | HCID 2734432 | — |
| Product | HCID 178422981 | HCID 178422981 | 51.8% |
Reaction Steps
A mixture of 2-Amino-6-methyl-nicotinic acid (1.44 g, 9.46 mmol) and formamide (8.0 g, 178 mmol) was stirred at 170° C. for 2 hours. After cooling, the mixture was quenched with water (4 mL). The precipitate was filtered, washed with water and dried to afford 7-Methyl-pyrido[2,3-d]pyrimidin-4-ol (0.79 g, 51%). 1H NMR (CDCl3, 400 MHz) δ 8.49 (d, J=8.4 Hz, 1H), 8.22 (s, 1H), 7.35 (d, J=8.0 Hz, 1H), 2.75 (s, 3H). MS (APCI+) [M+H]+162.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680114B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-ff22f0f053b149e48bd5673727901ea3 |
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| Source note | uspto-grants-2014_03 |
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