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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantHCID 19375609HCID 19375609—
Reactant4-(2-(4-Aminophenoxy)pyridin-3-yl)pyrimidin-2-amineHCID 57756218—
SolventDiethyl EtherHCID 3283—
SolventSodium CarbonateHCID 10340—
ProductN-(4-((3-(2-Amino-4-pyrimidinyl)-2-pyridinyl)oxy)phenyl)-4-(4-methyl-2-thienyl)-1-phthalazinamineHCID 24856041—

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921367B2
Source datasetuspto-grants-2014_12
ORD IDord-fbbe2d21b6c549e798fa5b473ce09ab8
Source noteuspto-grants-2014_12