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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 553512Erstellt: 25. Oktober 2026

Acetone → 1,3-Dimethyl-1H-pyrazole-4-sulfonic acid {2-[3'-(4-methoxymethyl-phenyl)-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-yl]-ethyl}-methyl-amide hydrochloride

https://huagongshe.com/reaction/553512

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktPotassium CarbonateHCID 11430—
Edukt4-(Methoxymethyl)benzeneboronic acidHCID 3723812—
Edukt1,3-Dimethyl-1H-pyrazole-4-sulfonic acid [2-(3'-chloro-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-yl)-ethyl]-methyl-amideHCID 86640205—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelN,N-Dimethylacetamide--water (1/1)HCID 21534740—
Produkt1,3-Dimethyl-1H-pyrazole-4-sulfonic acid {2-[3'-(4-methoxymethyl-phenyl)-2,3,5,6-tetrahydro-[1,2']bipyrazinyl-4-yl]-ethyl}-methyl-amide hydrochlorideHCID 6736957356%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

Dissolve 1,3-dimethyl-1H-pyrazole-4-sulfonic acid [2-(3′-chloro-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-yl)-ethyl]-methyl-amide (270 mg, 0.652 mmol) in DMA-H2O (10 ml; 3:1 v/v, previously degassed with nitrogen). Add 4-methoxymethylphenyl boronic acid (130 mg, 0.783 mmol), potassium carbonate (216 mg, 1.56 mmol) and tetrakis(triphenylphosphine)palladium (38 mg, 0.0326 mmol). Heat the reaction mixture at 110° C. for 18 hr. Cool and dilute with ethyl acetate and water. Extract the aqueous layer with ethyl acetate and combine the organic layers. Wash the organic layers with brine and concentrate. Purify by chromatography, eluting with 1:2 hexanes:acetone to afford the free base of the title compound (182 mg, 56% yield) as a white foam.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08048884B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-ef06884c375a45bd8abce15dfac76025
Quellennotizuspto-grants-2011_11