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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130442Erstellt: 25. Oktober 2026

4-Methylthiophene-2-boronic acid → HCID 59007070, Verbindung

https://huagongshe.com/reaction/130442

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Methylthiophene-2-boronic acidHCID 2734373—
EduktPotassium tert-butoxideHCID 23665647—
Edukt4-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]benzenesulfonamideHCID 44452776—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktHCID 59007070HCID 59007070—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a mixture of 4-bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]benzenesulfonamide (E106) (100 mg, 0.22 mmol) and (4-methyl-2-thienyl)boronic acid (71 mg, 0.50 mmol) in DME (3 ml) was added potassium tert-butoxide (220 mg, 1.96 mmol) and tetrakis(triphenylphosphine)palladium(0) (15 mg, 0.01 mmol) in water (1 ml) and the resulting mixture stirred in a microwave (set at high absorbance) at 100° C. for 30 minutes. The resulting mixture was then evaporated in vacuo and purified using an SCX cartridge eluting with methanol followed by ammonia (2M in methanol). The appropriate fractions were combined and solvent evaporated in vacuo and the residue purified further by mass directed autoprep HPLC to afford the title compound (E107). MS (ES+) m/e 472 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381728B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-54c353fc63094d949f46eadf9835d2d8
Quellennotizuspto-grants-2008_06