Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803607Generated: October 28, 2026

Binap, (A+-)- → HCID 58447309, compound

https://huagongshe.com/reaction/1803607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant(3-Pyrrolidin-1-ylphenyl)methylamineHCID 7162061—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 58447309HCID 584473094%

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (200 mg, 0.770 mmol), (3-pyrrolidin-1-ylphenyl)methylamine (149 mg, 0.848 mmol), Pd2(dba)3 (71 mg, 0.077 mmol), rac-BINAP (153 mg, 0.246 mmol) and NaOtBu (200 mg, 2.081 mmol) in DMA (6 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 (Hexanes/EtOAc) afforded 4-chloro-6-(3-pyrrolidin-1-yl-benzylamino)-2H-phthalazin-1-one (11 mg) as a white solid. 1H (400 MHz, d6-DMSO) δ: 1.94 (m, 4H), 3.20 (m, 4H), 4.32 (d, 2H), 6.41 (d, 1H), 6.57 (s, 1H), 6.60 (d, 1H), 6.85 (s, 1H), 7.11 (t, 1H), 7.15 (dd, 1H), 7.62 (t, 1H), 7.01 (d, 1H), 12.33 (s, 1H) ppm; m/z (M+1) 355.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349836B2
Source datasetuspto-grants-2013_01
ORD IDord-eed07bf24e9a45a5b69f108ac51c612b
Source noteuspto-grants-2013_01