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HRID 220533Erstellt: 25. Oktober 2026

Water → 4-(1,3-Dimethyl-1H-pyrazol-4-ylmethyl)-3'-(4-chloro-3-fluorophenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazine

https://huagongshe.com/reaction/220533

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
Edukt4-Chloro-3-fluorophenylboronic AcidHCID 2778656—
Edukt3'-Chloro-4-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazineHCID 86641656—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-(1,3-Dimethyl-1H-pyrazol-4-ylmethyl)-3'-(4-chloro-3-fluorophenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazineHCID 5932176314%

Reaktionsschritte

Add 4-chloro-3-fluorobenzeneboronic acid (125 mg, 0.72 mmol) to a nitrogen purged solution of 3′-chloro-4-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (200 mg, 0.65 mmol) in dry N,N-dimethylacetamide (4 mL) and deoxygenated water (2 mL). Add potassium carbonate (215 mg, 1.72 mmol) then tetrakis(triphenylphosphine)palladium(0) (0.004 g, 0.0035 mmol) and stir at 110° C. for 6 hr. Cool to room temperature, add water (10 mL) and extract with DCM (3×20 mL). Concentrate the combined DCM extracts and purify by reverse phase HPLC to give the title compound (0.036 g, 14%). MS (ES): m/z=401 [M+H]+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202873B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-36626122de3d4f8682d0e2eb4b099977
Quellennotizuspto-grants-2012_06