Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667433Generated: October 25, 2026

2-Chloro-6-fluorobenzylamine → 4-Chloro-6-(2-chloro-6-fluoro-benzylamino)-2H-phthalazin-1-one

https://huagongshe.com/reaction/1667433

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-fluorobenzylamineHCID 84833—
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—
Product4-Chloro-6-(2-chloro-6-fluoro-benzylamino)-2H-phthalazin-1-oneHCID 58447269—

Reaction Steps

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 2-chloro-6-fluoro-benzylamine (102 mg, 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-chloro-6-fluoro-benzylamino)-2H-phthalazin-1-one: 31 mg (15.8%): m/z (M+H)=338. 1H-NMR (DMSO-d6) δ: 12.38 (s, 1H), 7.94 (d, 1H), 7.42 (m, 3H), 7.30 (m, 1H), 7.21 (dd, 1H) 6.93 (s, 1H), 4.49 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044041B2
Source datasetuspto-grants-2011_10
ORD IDord-caa092d17732480aac541929867c8a05
Source noteuspto-grants-2011_10