Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803540Generated: October 31, 2026

2,5-Dimethylbenzylamine → HCID 24945980, compound

https://huagongshe.com/reaction/1803540

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DimethylbenzylamineHCID 66735—
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 24945980HCID 24945980—

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 2,5-dimethyl-benzylamine (87 mg, 0.64 mmol), Pd2(dba)3 (53 mg, 0.058 mmol), rac-BINAP (132 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-dimethyl-benzylamino)-2H-phthalazin-1-one: 31 mg (17.0%): m/z (M+H)=314. 1H-NMR (DMSO-d6) δ: 12.34 (s, 1H), 7.92 (d, 1H), 7.45 (m, 1H), 7.16 (dd, 1H), 7.10 (m, 2H), 6.99 (m, 1H), 6.85 (s, 1H), 4.32 (d, 2H), 2.29 (s, 3H), 2.22 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349836B2
Source datasetuspto-grants-2013_01
ORD IDord-151bf857a4404037b900c292fc97124e
Source noteuspto-grants-2013_01