Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357583Generated: October 31, 2026

Potassium Carbonate → N-cyclopropyl-4-methyl-3-(1-(3-oxopiperazin-1-yl)phthalazin-6-yl)benzamide

https://huagongshe.com/reaction/2357583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamideHCID 21914577—
Reactant4-(6-Bromophthalazin-1-yl)piperazin-2-oneHCID 68455278—
CatalystHCID 178418397HCID 178418397—
SolventDimethoxyethane ethanolHCID 20074477—
ProductN-cyclopropyl-4-methyl-3-(1-(3-oxopiperazin-1-yl)phthalazin-6-yl)benzamideHCID 1184824584%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-(6-bromophthalazin-1-yl)piperazin-2-one (0.10 g, 326 μmol), N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (98mg, 326 μmol), and tetrakis(triphenylphosphine)palladium (19 mg, 16 μmol) in 5 mL DME/EtOH (4:1) was treated with 2M potassium carbonate (488 μl, 977 μmol). The resulting mixture was warmed up to 90° C. and stirred for 1 h under nitrogen. The mixture was cooled to room temperature, and the crude product was purified via flash chromatography (silica gel) eluting with a gradient of 4% 2 M ammonia in MeOH/DCM to 6% 2 M ammonia in MeOH/DCM to give the title compound (0.11 g) as a pale yellow solid. Found MS(ES+): 402(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-3e39f7ebe9c44c18835196d9e8bb646f
Source noteuspto-grants-2010_07