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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzo(b)thiophene, 3-bromo- | HCID 123250 | — |
| Edukt | 1-(4-Aminobenzoyl)-3-dimethylamino-pyrrolidine | HCID 22567471 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Katalysator | HCID 178454872 | HCID 178454872 | — |
| Produkt | 1-[4-(1-Benzothien-3-ylamino)benzoyl]-N,N-dimethylpyrrolidin-3-amine | HCID 24794879 | 14,3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07842715B2 |
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| Quelldatensatz | uspto-grants-2010_11 |
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| ORD ID | ord-836d361ff6cb4c1fb9960d8ed8864ed9 |
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| Quellennotiz | uspto-grants-2010_11 |
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