Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1176060Erstellt: 26. Oktober 2026

Benzo(b)thiophene, 3-bromo- → 1-[4-(1-Benzothien-3-ylamino)benzoyl]-N,N-dimethylpyrrolidin-3-amine

https://huagongshe.com/reaction/1176060

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzo(b)thiophene, 3-bromo-HCID 123250—
Edukt1-(4-Aminobenzoyl)-3-dimethylamino-pyrrolidineHCID 22567471—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
KatalysatorHCID 178454872HCID 178454872—
Produkt1-[4-(1-Benzothien-3-ylamino)benzoyl]-N,N-dimethylpyrrolidin-3-amineHCID 2479487914,3%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 1-(4-aminobenzoyl)-3-dimethylamino-pyrrolidine (50 mg, 0.21 mmol), 3-bromobenzothiophene (50 mg, 0.23 mmol), sodium tert-butoxide (44 mg, 34 mmol), tris(dibenzylideneacetone)dipalladium(0) (3 mg, 0.002 mmol), CTC-Q-Phos (6 mg, 0.004 mmol) is heated to 80° C. for 16 h and concentrated in vacuo. The resultant residue is dissolved in a mixture of DMSO, methanol and water and purified by reverse-phase semi-preparative HPLC1 to give the title compound as a white powder (11 mg), identified by HPLC and mass spectral analyses. Retention Time, 2.62 min.; MS [366.2 m/e (M+H)]. 1Semi-preparative HPLC Conditions: A=0.02% TFA in water, B=0.02% TFA in acetonitrile, 10-95% B in 8 min., 34 mL/min, 50° C., 215 nm detection, Waters Xterra™ 20×50 mm column.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07842715B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-836d361ff6cb4c1fb9960d8ed8864ed9
Quellennotizuspto-grants-2010_11