HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408504Generated: October 31, 2026
tert-Butanol → N-(4-((3-(2-Amino-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-4-(4-methyl-2-thienyl)-1-phthalazinamine
https://huagongshe.com/reaction/1408504
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | HCID 19375609 | HCID 19375609 | — |
| Reactant | 4-(2-(4-Aminophenoxy)pyridin-3-yl)pyrimidin-2-amine | HCID 57756218 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | N-(4-((3-(2-Amino-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-4-(4-methyl-2-thienyl)-1-phthalazinamine | HCID 24856041 | — |
Reaction Steps
To 4-(2-(4-aminophenoxy)pyridin-3-yl)pyrimidin-2-amine and 1-chloro-4-(4-methyl-2-thienyl)phthalazine was added tBuOH. 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-amino-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-4-(4-methyl-2-thienyl)-1-phthalazinamine as an off-white solid. MS m/z=504 [M+H]+. Calc'd for C28H21N7OS: 503.58.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921367B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-fbbe2d21b6c549e798fa5b473ce09ab8 |
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| Source note | uspto-grants-2014_12 |
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