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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1667453Erstellt: 26. Oktober 2026

Binap, (A+-)- → 4-Chloro-6-(2-chloro-6-phenoxy-benzylamino)-2H-phthalazin-1-one

https://huagongshe.com/reaction/1667453

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBinap, (A+-)-HCID 634876—
Edukt2-Chloro-6-phenoxybenzylamineHCID 2777206—
EduktSodium t-butoxideHCID 23676156—
Edukt6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-Chloro-6-(2-chloro-6-phenoxy-benzylamino)-2H-phthalazin-1-oneHCID 24945981—

Reaktionsschritte

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 2-chloro-6-phenoxy-benzylamine (150 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-chloro-6-phenoxy-benzylamino)-2H-phthalazin-1-one: 39 mg (16.3%): m/z (M+H)=412. 1H-NMR (DMSO-d6) δ: 12.34 (s, 1H), 7.90 (d, 1H), 7.35 (m, 5H), 7.21 (dd, 1H), 7.15 (m, 1H), 7.02 (m, 2H), 6.95 (d, 1H), 6.84 (dd, 1H), 4.50 (d, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08044041B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-b21b5a2bd13a43ae9f3fbfd22e681839
Quellennotizuspto-grants-2011_10