HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361046Generated: October 25, 2026
tert-Butanol → N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenylphthalazin-1-amine
https://huagongshe.com/reaction/2361046
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 1-Chloro-4-phenylphthalazine | HCID 272109 | — |
| Reactant | 4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyridin-2-amine | HCID 66735161 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenylphthalazin-1-amine | HCID 57756271 | — |
Reaction Steps
To 4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyridin-2-amine (0.070 g, 0.24 mmol) and 1-chloro-4-phenylphthalazine (0.048 g, 0.20 mmol) was added tBuOH (1.0 mL). The resulting mixture was heated at 100° C. in a sealed tube for 16 hours. The reaction was diluted with diethyl ether and saturated sodium carbonate and vigorously shaken. The resulting solids were filtered and washed with water, diethyl ether and air dried to yield N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenylphthalazin-1-amine as an off-white solid. MS m/z=497 [M+H]+. Calc'd for C31H24N6O: 496.58.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686155B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-e396a48e028243ec828c936e5857f4be |
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| Source note | uspto-grants-2014_04 |
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