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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803564Generated: October 31, 2026

Binap, (A+-)- → 4-chloro-6-(2-pyrrol-1-yl-benzylamino)-2H-phthalazin-1-one

https://huagongshe.com/reaction/1803564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant2-(1-Pyrrolyl)benzylamineHCID 707327—
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-pyrrol-1-yl-benzylamino)-2H-phthalazin-1-oneHCID 2494834416.3%

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.578 mmol), 2-(1-pyrrolyl)benzylamine (122 mg, 0.708 mmol), Pd2(dba)3 (56 mg, 0.061 mmol), rac-BINAP (108 mg, 0.173 mmol) and NaOtBu (139 mg, 1.445 mmol) in DMA (5 mL) was heated at 85° C. for 1.5 h. The mixture was allowed to cool, diluted with EtOAc and washed with water. The organic layer was washed with sat.aq. NaHCO3, brine and dried (Na2SO4). Chromatography on silica (EtOAc/hexanes) afforded 4-chloro-6-(2-pyrrol-1-yl-benzylamino)-2H-phthalazin-1-one (33 mg) as an off white solid, 1H (400 MHz, d6-DMSO) δ: 4.22 (d, 2H), 6.26 (t, 2H), 6.60 (bs, 1H), 7.04 (t, 2H), 7.08 (d, 1H), 7.35 (m, 1H), 7.40 (m, 2H), 7.49 (m, 1H), 7.62 (t, 1H), 7.91 (d, 1H) ppm; m/z (M+1) 350.97.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349836B2
Source datasetuspto-grants-2013_01
ORD IDord-0db48c9f2cd740058260d7a286457bb8
Source noteuspto-grants-2013_01