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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1667428Erstellt: 25. Oktober 2026

Binap, (A+-)- → 4-Chloro-6-(3-piperidin-1-ylmethyl-benzylamino)-2H-phthalazin-1-one

https://huagongshe.com/reaction/1667428

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBinap, (A+-)-HCID 634876—
Edukt3-Piperidin-1-ylmethyl-benzylamineHCID 2794678—
EduktSodium t-butoxideHCID 23676156—
Edukt6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-Chloro-6-(3-piperidin-1-ylmethyl-benzylamino)-2H-phthalazin-1-oneHCID 58447352—

Reaktionsschritte

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (70 mg, 0.27 mmol), 3-piperidin-1-ylmethyl-benzylamine (72 mg, 0.35 mmol), Pd2(dba)3 (25 mg, 0.027 mmol), rac-BINAP (51 mg, 0.081 mmol) and NaOt-Bu (76 mg, 0.81 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-(3-piperidin-1-ylmethyl-benzylamino)-2H-phthalazin-1-one: 16 mg (15.5%): m/z (M+H)=383. 1H-NMR (DMSO-d6) δ: 12.30 (s, 1H), 7.95 (d, 1H), 7.63 (m, 1H), 7.25 (m, 3H), 7.15 (m, 2H), 6.75 (s, 1H), 4.41 (d, 2H), 3.37 (s, 2H), 2.24 (m, 4H), 1.38 (m, 4H), 1.32 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08044041B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-abf262d810e54e39bd412ecdac26a62c
Quellennotizuspto-grants-2011_10