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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667431Generated: October 25, 2026

Benzenemethanamine, 2,5-dichloro- → HCID 58447324, compound

https://huagongshe.com/reaction/1667431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenemethanamine, 2,5-dichloro-HCID 457600—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactant6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 58447324HCID 58447324—

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 2,5-dichloro-benzylamine (0.085 mL, 0.64 mmol), Pd2(dba)3 (53 mg, 0.058 mmol), rac-BINAP (108 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-(2,5-dichloro-benzylamino)-2H-phthalazin-1-one: 6 mg (2.9%): m/z (M+H)=354. 1H-NMR (DMSO-d6) δ: 12.39 (s, 1H), 7.96 (d, 1H), 7.66 (m, 1H), 7.53 (d, 1H), 7.47 (m, 1H), 7.40 (dd, 1H), 7.16 (dd, 1H), 6.82 (s, 1H), 4.50 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044041B2
Source datasetuspto-grants-2011_10
ORD IDord-c1d9ebd9553347a6a878c13c4ce82117
Source noteuspto-grants-2011_10