HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 218212Erstellt: 25. Oktober 2026
(Trifluoromethyl)trimethylsilane → HCID 57377969, Verbindung
https://huagongshe.com/reaction/218212
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | (Trifluoromethyl)trimethylsilane | HCID 552549 | — |
| Edukt | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Edukt | 4-acetyl-N-(4-chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)benzenesulfonamide | HCID 57378404 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | HCID 57377969 | HCID 57377969 | — |
Reaktionsschritte
To 4-acetyl-N-(4-chloro-2-[1,2,3]triazolo[4,5-b]pyridin-1-yl-phenyl)-benzene-sulfonamide (synthesized according to general procedures F and G, 500 mg, 1.17 mmol) was added CF3-TMS (trifluoromethyl-trimethylsilane) (4.7 mL, 0.5 M solution in THF), followed by TBAF (tetra-n-butylammonium fluoride) (2.34 mL, 1.0 M solution in THF) at 0° C., and the solution was stirred at room temperature for 16 hours. Both TLC and LCMS analysis indicated ˜10-15% completion of reaction. The reaction mixture was diluted with EtOAc (50 mL) and the organics were washed with washed with 2 N HCl (2×25 mL), water (25 mL), and brine (25 mL). The organics were subsequently dried (Na2SO4), concentrated in vacuo, and purified by automated flash chromatography followed by preparative HPLC to afford the title compound as a white powder: MS (ES) M+H expected 498.1, found 498.0.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08198309B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-e84ea3eb6e3f4e04b2319103f4348481 |
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| Quellennotiz | uspto-grants-2012_06 |
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