Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689974Generated: October 26, 2026

Potassium Phosphate, Tribasic → (R)-4-(4-(4-benzoyl-2-methylpiperazin-1-yl)phthalazin-1-yl)benzamide

https://huagongshe.com/reaction/1689974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Aminocarbonylphenylboronic acidHCID 2737811—
ReactantDicyclohexyl(2,6-dimethoxyphenyl)phosphineHCID 57474835—
Reactant(R)-(4-(4-chlorophthalazin-1-yl)-3-methylpiperazin-1-yl)(cyclohexyl)methanoneHCID 57581516—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product(R)-4-(4-(4-benzoyl-2-methylpiperazin-1-yl)phthalazin-1-yl)benzamideHCID 49862220—

Reaction Conditions

Temperature100 °C

Reaction Steps

Compound 71 was prepared according to general method H. A 15 mL Schlenk tube was charged with (R)-(4-(4-chlorophthalazin-1-yl)-3-methylpiperazin-1-yl)(cyclohexyl)methanone JK-5 (130 mg, 349 μmol), 4-carbamoylphenylboronic acid (77 mg, 523 μmol), tris(dibenzylideneacetone)dipalladium (0) (3.2 mg, 3.5 μmol), dicyclohexyl(2,6-dimethoxyphenyl)phosphine (2.3 mg, 7.0 μmol), and potassium phosphate tribasic (148 mg, 697 μmol). The vessel was evacuated, backfilled with argon 5 times, and then previously degassed n-butanol (1 mL) was added. The reaction was heated at 100° C. for 20 hours. After cooling, the reaction was added to aqueous K2CO3 (10%) and extracted three times with dichloromethane. The combined organics were dried (MgSO4) and evaporated to give a yellow oil. Chromatography over silica gel with a gradient of hexanes/0-100% ethyl acetate gave a pale yellow solid, compound 71. MS (M+H)+=452.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153633B2
Source datasetuspto-grants-2012_04
ORD IDord-4afedb6ebee045749f1a752944c8deea
Source noteuspto-grants-2012_04