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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667444Generated: October 26, 2026

Binap, (A+-)- → 4-Chloro-6-[2-(4-methyl-piperazin-1-yl)-benzylamino]-2H-phthalazin-1-one

https://huagongshe.com/reaction/1667444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant2-(4-Methyl-1-piperazinyl)benzenemethanamineHCID 2795568—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product4-Chloro-6-[2-(4-methyl-piperazin-1-yl)-benzylamino]-2H-phthalazin-1-oneHCID 24946338—

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 2-(4-methyl-piperazin-1-yl)-benzylamine (132 mg, 0.64 mmol), Pd2(dba)3 (53 mg, 0.058 mmol), rac-BINAP (132 mg, 0.17 mmol) and NaOt-Bu (140 mg, 1.45 mmol) in DMA (6 mL) was heated at 80° C. for 1 h. The mixture was allowed to cool, diluted with EtOAc (25 mL) and washed with water (25 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated. Chromatography on silica (EtOAc/hexanes) yielded the title compound. 4-Chloro-6-[2-(4-methyl-piperazin-1-yl)-benzylamino]-2H-phthalazin-1-one: 46 mg (20.7%): m/z (M+H)=384. 1H-NMR (DMSO-d6) δ: 12.31 (s, 1H), 7.89 (d, 1H), 7.77 (m, 1H), 7.33 (dd, 1H), 7.20 (m, 1H), 7.13 (m, 2H), 7.00 (m, 1H), 6.63 (s, 1H), 4.42 (d, 2H), 2.98 (m, 4H), 2.52 (m, 4H), 2.23 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044041B2
Source datasetuspto-grants-2011_10
ORD IDord-5ca1677eb7ec4adfaada18f4a2b91663
Source noteuspto-grants-2011_10