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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803527Generated: November 1, 2026

Binap, (A+-)- → HCID 24946341, compound

https://huagongshe.com/reaction/1803527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant1-[3-(4-Methylpiperazin-1-yl)phenyl]methanamineHCID 4961252—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 24946341HCID 24946341—

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 3-(4-methyl-piperazin-1-yl)-benzylamine (111 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-[3-(4-methyl-piperazin-1-yl)-benzylamino]-2H-phthalazin-1-one: 50 mg (22.5%): m/z (M+H)=384. 1H-NMR (DMSO-d6) δ: 12.33 (s, 1H), 7.91 (d, 1H), 7.59 (m, 1H), 7.16 (m, 2H), 6.98 (s, 1H), 6.80 (m, 3H), 4.34 (d, 2H), 3.11 (m, 4H), 2.42 (m, 4H), 2.20 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349836B2
Source datasetuspto-grants-2013_01
ORD IDord-9be9403f2e514894bce69eefbfddda53
Source noteuspto-grants-2013_01