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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911140Generated: 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/911140

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant1-Chloro-4-phenylphthalazineHCID 272109—
Reactant4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyridin-2-amineHCID 66735161—
SolventDiethyl EtherHCID 3283—
SolventSodium CarbonateHCID 10340—
ProductN-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenylphthalazin-1-amineHCID 57756271—

Reaction Conditions

Temperature100 °C

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-phenyphthalazin-1-amine as an off-white solid. MS m/z=497 [M+H]+. Calc'd for C31H24N6O: 496.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022221B2
Source datasetuspto-grants-2011_09
ORD IDord-6f281ca63e6d49828b92ec9c6648cbb2
Source noteuspto-grants-2011_09