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HRID 1667492Erstellt: 25. Oktober 2026

Binap, (A+-)- → 4-chloro-6-(2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-yl)-2H-phthalazin-1-one

https://huagongshe.com/reaction/1667492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBinap, (A+-)-HCID 634876—
Edukt1-PiperazinylpyrazineHCID 2734639—
EduktSodium t-butoxideHCID 23676156—
Edukt6-Bromo-4-chlorophthalazin-1(2H)-oneHCID 53308487—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-chloro-6-(2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-yl)-2H-phthalazin-1-oneHCID 2494703516,7%

Reaktionsschritte

A mixture 6-bromo-4-chloro-2H-phthalazin-1-one (145 mg, 0.559 mmol), 1-(2-pyrazinyl)piperazine (104 mg, 0.633 mmol), Pd2(dba)3 (43 mg, 0.047 mmol), rac-BINAP (116 mg, 0.186 mmol) and NaOtBu (167 mg, 1.738 mmol) in DMA (5 mL) was heated at 85° C. for 1.5 h. The mixture was allowed to cool, diluted with EtOAc and washed with water. The organic layer was washed with sat.aq. NaHCO3, brine and dried (Na2SO4). Preparatory HPLC afforded 4-chloro-6-(2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-yl)-2H-phthalazin-1-one (32 mg) as a yellow solid, 1H (400 MHz, d6-DMSO) δ: 3.62 (m, 4H), 3.78 (m, 4H), 7.12 (d, 1H), 7.60 (dd, 1H), 7.87 (d, 1H), 8.07 (d, 1H), 8.11 (m, 1H), 8.37 (s, 1H), 12.51 (s, 1H) ppm. m/z (M+1) 342.98.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08044041B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-f67a6f891ef740a7aae88db4dddbf12e
Quellennotizuspto-grants-2011_10