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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357636Generated: October 30, 2026

Water → 4-Chloro-3-(1-morpholin-4-ylphthalazin-6-yl)benzamide

https://huagongshe.com/reaction/2357636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant4-Chloro-3-iodobenzamideHCID 22115576—
Reactant6-Bromo-1-morpholinophthalazineHCID 25129478—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product4-Chloro-3-(1-morpholin-4-ylphthalazin-6-yl)benzamideHCID 68456728—

Reaction Conditions

Temperature80 °C

Reaction Steps

To 6-Bromo-1-morpholinophthalazine (0.20 g, 680 μmol), 1,1′-bis(diphenylphosphino)ferrocene-palladium dichloride (50 mg, 68 μmol), potassium acetate (200 mg, 2040 μmol), and 4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane (207 mg, 816 μmol) was added 1,4-dioxane (6.80 mL) and the mixture was heated to 80° C. for 2 h. The mixture was added to a sealed tube containing 4-chloro-3-iodobenzamide (230 mg, 816 μmol), tetrakis(triphenylphosphine)palladium (79 mg, 68 μmol), potassium carbonate—1.5 M in water (1.81 μl, 2.72 mmol), and ethanol (6.80 mL) and heated to 110° C. for 2 h. After cooling the reaction mixture was diluted with 75 mL of ethyl acetate, added to a separation funnel, partitioned with sodium bicarbonate (saturated, aqueous), washed 3 times with 50 mL of sodium bicarbonate (saturated, aqueous), separated, dried over sodium sulfate, concentrated in vacuo, and purified by HPLC to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-ac43cb98b6b340debbd465fa1b976610
Source noteuspto-grants-2010_07