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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012975Generated: November 3, 2026

1-(4-Fluorophenyl)piperazine → HCID 59833503, compound

https://huagongshe.com/reaction/1012975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3-((4-Oxo-3,4-dihydrophthalazin-1-yl)methyl)benzoic acidHCID 25131906—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductHCID 59833503HCID 5983350347.7%

Reaction Steps

2-(1H-Benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (150 mg, 0.47 mmol), diisopropylethylamine (102 mg, 0.8 mmol) and 1-(4-fluorophenyl)piperazine (65 mg, 0.47 mmol) were added sequentially at ambient temperature to a stirred solution of 3-(4-oxo-3,4-dihydrophthalazin-1-ylmethyl)benzoic acid (A) (100 mg, 0.36 mmol) in dry dimethylacetamide (1 ml), the mixture was stirred at ambient temperature for 4 hours and allowed to stand at ambient temperature for 16 hours, then it was added dropwise to stirred cold water (10 ml). After 30 minutes, the resulting solid was collected by filtration, washed with water (2×1 ml) and hexane (1 ml), dried in vacuo and purified using preparative HPLC to give 4-{3-[4-(4-fluorophenyl)piperazin-1-ylcarbonyl]benzyl}-1(2H)-phthalazinone (21) (76 mg) as a cream solid; m/z (M+H)+• 443; HPLC Purity 90%; HPLC Retention time 4.00 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981889B2
Source datasetuspto-grants-2011_07
ORD IDord-7a58d40342674a34a9d16d4f6426c355
Source noteuspto-grants-2011_07