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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803533Generated: October 31, 2026

Binap, (A+-)- → HCID 24946165, compound

https://huagongshe.com/reaction/1803533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
ReactantHCID 66706804HCID 66706804—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 24946165HCID 24946165—

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), (2,3-dihydro-benzofuran-5-yl)-methylamine hydrochloride (119 mg, 0.64 mmol), Pd2(dba)3 (53 mg, 0.058 mmol), rac-BINAP (132 mg, 0.17 mmol) and NaOt-Bu (200 mg, 2.1 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-[(2,3-dihydro-benzofuran-5-ylmethyl)-amino]-2H-phthalazin-1-one: 25 mg (13.2%): m/z (M+H)=328. 1H-NMR (DMSO-d6) δ: 12.28 (s, 1H), 7.86 (d, 1H), 7.51 (m, 1H), 7.19 (s, 1H), 7.10 (dd, 1H), 7.05 (d, 1H), 6.78 (s, 1H), 6.67 (d, 1H), 4.44 (t, 2H), 4.26 (d, 2H), 3.09 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349836B2
Source datasetuspto-grants-2013_01
ORD IDord-2091dd3c57f647e6800e52732994b6c7
Source noteuspto-grants-2013_01