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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1803536Erstellt: 26. Oktober 2026

Binap, (A+-)- → 4-Chloro-6-(5-chloro-2-methyl-benzylamino)-2H-phthalazin-1-one

https://huagongshe.com/reaction/1803536

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBinap, (A+-)-HCID 634876—
Edukt5-Chloro-2-methylbenzylamineHCID 2757673—
EduktSodium t-butoxideHCID 23676156—
Edukt6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-Chloro-6-(5-chloro-2-methyl-benzylamino)-2H-phthalazin-1-oneHCID 24946162—

Reaktionsschritte

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (150 mg, 0.58 mmol), 5-chloro-2-methyl-benzylamine (100 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-(5-chloro-2-methyl-benzylamino)-2H-phthalazin-1-one: 20 mg (10.3%): m/z (M+H)=334. 1H-NMR (DMSO-d6) δ: 12.63 (s, 1H), 8.21 (d, 1H), 7.78 (m, 1H), 7.56 (m, 1H), 7.50 (m, 2H), 7.42 (dd, 1H), 7.10 (s, 1H), 4.66 (d, 2H), 2.60 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08349836B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-86a677dad01344c6b1438d75b3de2f57
Quellennotizuspto-grants-2013_01