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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803560Generated: November 1, 2026

Binap, (A+-)- → 4-chloro-6-(2,3-difluoro-benzylamino)-2H-phthalazin-1-one

https://huagongshe.com/reaction/1803560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant2,3-DifluorobenzylamineHCID 2736941—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product4-chloro-6-(2,3-difluoro-benzylamino)-2H-phthalazin-1-oneHCID 2494853214%

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (156 mg, 0.601 mmol), 2,3-difluorobenzylamine (0.074 mL, 0.646 mmol), Pd2(dba)3 (53 mg, 0.058 mmol), rac-BINAP (104 mg, 0.167 mmol) and NaOtBu (134 mg, 1.39 mmol) in DMA (6 mL) was heated at 80° 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-(2,3-difluoro-benzylamino)-2H-phthalazin-1-one (27 mg) as an off white solid, 1H (400 MHz, CDCl3) δ: 4.45 (s, 2H), 6.84 (d, 1H), 6.96 (m, 2H), 7.03 (m, 2H), 8.01 (d, 1H), 11.00 (s, 1H) ppm; m/z (M+1) 321.91.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349836B2
Source datasetuspto-grants-2013_01
ORD IDord-be7e568b98804b5eb2cef4d54faa9617
Source noteuspto-grants-2013_01