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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428919Generated: November 1, 2026

Nitrogen → HCID 67160967, compound

https://huagongshe.com/reaction/1428919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant4-chlorophthalazin-1(2H)-oneHCID 2775142—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67160967HCID 6716096785%

Reaction Steps

A solution of 1-chlorophthalazine-4-one (1.0 g, 5.5 mmol), 3-chlorophenyl boronic acid (1.3 g, 8.3 mmol), tricyclohexyphosphine (0.058 g, 0.27 mmol), and K3PO4 (2.3 g, 11.0 mmol) in THF (20 mL) and water (5 mL) was degassed with N2 for 30 min then treated with tri(dibenzylideneacetone)-dipalladium (0.050 g, 0.05 mmol) and heated at reflux overnight. The reaction mixture was diluted with water (100 mL) and the product extracted with EtOAc (2×100 mL). The organics were washed with brine, dried over Na2SO4, and concentrated to give 4-(3-chlorophenyl)phthalazin-1(2H)-one (1.2 g), (MS: ESI +ve, 257.12 [M+H]). 1H NMR: (400 MHz, DMSO) δ: 7.58-7.60 (m, 2H), 7.61-7.64 (m, 2H), 7.65-7.67 (m, 1H), 7.90-7.93 (m, 2H), 8.34-8.36 (m, 1H). 12.93 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937178B2
Source datasetuspto-grants-2015_01
ORD IDord-882b2cac2b384a949299ea9fea8fc7f4
Source noteuspto-grants-2015_01