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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357675Generated: November 1, 2026

Water → N-cyclopropyl-4-methyl-3-(1-(2-methyl-3-oxopiperazin-1-yl)phthalazin-6-yl)benzamide

https://huagongshe.com/reaction/2357675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantN-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamideHCID 21914577—
Reactant4-(6-Bromophthalazin-1-yl)-3-methylpiperazin-2-oneHCID 68453097—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductN-cyclopropyl-4-methyl-3-(1-(2-methyl-3-oxopiperazin-1-yl)phthalazin-6-yl)benzamideHCID 6845599248.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

This compound was prepared by a method analogous to that described in Example 8 (Method A). A mixture of 4-(6-bromophthalazin-1-yl)-3-methylpiperazin-2-one (0.200 g, 0.62 mmol), N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (0.245 g, 0.81 mmol), sodium carbonate (0.270 g, 2.5 mmol) and trans-dichlorobis(triphenyl-phosphine)palladium (II) (0.040 g, 0.050 mmol) in DME (7 mL)/H2O (3 mL)/EtOH (2 mL) was heated at 90° C. The reaction was purified by flash chromatography eluting with 2M NH3 in MeOH/CH2Cl2 (0:1-1:19) to give 126 mg of a brown amorphous solid. The material was further purified by reverse phase HPLC (10→100% CH3CN [0.1% TFA]) to give the title compound as a light yellow amorphous solid. Found MS m/z: 416.2 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-59152d2db42844fa911d46de78872237
Source noteuspto-grants-2010_07