Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 71245036 | HCID 71245036 | — |
| Reactant | HCID 178419482 | HCID 178419482 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178518691 | HCID 178518691 | 40.4% |
Reaction Steps
A mixture of (R)-3-(5-fluoro-4-(piperidin-3-ylamino)pyrimidin-2-ylamino)pyridin-2(1H)-one (Preparation 22c, 50 mg, 0.16 mmol) and 3-bromo-4H-1,2,4-triazole (prepared as described in J. Med. Chem. 2004, 47(19), 4645, 12.2 mg, 0.08 mmol) was stirred and heated overnight at 150° C. The reaction mixture was cooled to ambient temperature and diluted with methanol. Diethyl ether was then added and the precipitate that formed was filtered. The filtrate was concentrated under reduced pressure and the resulting semisolid was suspended in diethyl ether and filtered to yield the title compound (12 mg, 40%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034311B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-e1f861fd030442b79ff47bfa383b22fe |
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| Source note | uspto-grants-2015_05 |
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