Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357585Generated: October 31, 2026

Potassium Carbonate → 3-(1-(2-chlorophenyl)phthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide

https://huagongshe.com/reaction/2357585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chlorophenylboronic acidHCID 2734322—
Reactant3-(1-chlorophthalazin-6-yl)-N-cyclopropyl-4-methylbenzamideHCID 11848312—
CatalystHCID 178418397HCID 178418397—
SolventDimethoxyethane ethanolHCID 20074477—
Product3-(1-(2-chlorophenyl)phthalazin-6-yl)-N-cyclopropyl-4-methylbenzamideHCID 1184837221.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3-(1-chlorophthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide (0.11 g, 0.327 mmol), 2-chlorophenylboronic acid (51 mg, 329 μmol), 5 mL DME/EtOH (4:1), 0.5 mL 2M K2CO3 and tetrakis(triphenylphosphine)palladium (20mg) was stirred at 90° C. for 1 h. The reaction mixture was cooled to RT. The crude product was purified via flash chromatography (silica gel) with 2% 2 M ammonia in MeOH/DCM to 6% 2 M ammonia in MeOH/DCM to give the crude compound (120 mg) as a yellow solid. The compound was further purified by HPLC by dissolving the crude product in methanol (˜20 mg/mL) and injecting at a rate of about 0.500 mL per injection onto the Gilson preparatory HPLC. Pure product fractions were collected, combined, basefied with sodium bicarbonate (saturated, aqueous), extracted with CH2Cl2, separated, dried over sodium sulfate, and concentrated via rotary evaporation to give pure title compound (28.8 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-640f421a670d477684b97200e0f9bd63
Source noteuspto-grants-2010_07