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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911138Generated: October 30, 2026

1,4-Dichloro-5,6,7,8-tetrahydrophthalazine → 4-chloro-N-(4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)-5,6,7,8-tetrahydrophthalazin-1-amine

https://huagongshe.com/reaction/911138

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dichloro-5,6,7,8-tetrahydrophthalazineHCID 12622440—
Reactant4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyrimidin-2-amineHCID 46929541—
SolventMethanolHCID 887—
Product4-chloro-N-(4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)-5,6,7,8-tetrahydrophthalazin-1-amineHCID 57756230—

Reaction Steps

A slurry of 1,4-dichloro-5,6,7,8-tetrahydrophthalazine (1.66 g, 8.18 mmol) and 4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyrimidin-2-amine (2.00 g, 6.82 mmol) in 14 mL 2-BuOH was heated in a sealed pressure vessel to 110° C. The reaction became a thick mass that eventually became a stirring suspension over about 30 min. After 4 h, the reaction was cooled to ambient temperature, and the material was partitioned between 2N NaOH and EtOAc. The aqueous layer was extracted once with EtOAc. The organic layers were dried over anhyd. sodium sulfate, filtered, and concentrated to yield a brown solid. This solid was dissolved in MeOH/MC and adsorbed onto 10 g silica gel, dried, and purified by chromatography (0-100% EtOAc/DCM) to give 4-chloro-N-(4-(3-(2-(methylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)-5,6,7,8-tetrahydrophthalazin-1-amine as an off-white solid. MS m/z=460 [M+H]+. Calc'd for C24H22ClN7O: 459.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022221B2
Source datasetuspto-grants-2011_09
ORD IDord-ca3b9548a2194939aaf03e71124ad2df
Source noteuspto-grants-2011_09