Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | HCID 18361871 | HCID 18361871 | — |
| Reactant | 4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyrimidin-2-amine | HCID 46929541 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57756224 | HCID 57756224 | — |
Reaction Steps
To 4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyrimidin-2-amine (0.100 g, 0.34 mmol) and 1,4-dichloro-5,8-difluorophthalazine (0.096 g, 0.41 mmol) was added tBuOH (1.0 mL). The resulting mixture was heated to 100° C. in a sealed tube for 45 min. The reaction was diluted with diethyl ether and the resulting solids were filtered and triturated with EtOAc. The solids were dried to yield 4-chloro-5,8-difluoro-N-(4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)phthalazin-1-amine as a dark gray solid. MS m/z=492 [M+H]+. Calc'd for C24H16ClF2N7O: 491.89.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242961B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-febcf8aee34d444db5670f263e5be14e |
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| Source note | uspto-grants-2016_01 |
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