HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1054681Erstellt: 25. Oktober 2026
Ethyl Acetate → methyl 6-chloro-5-{4-[2-(piperazin-1-yl)ethoxy]phenyl}-1H-indole-3-carboxylate
https://huagongshe.com/reaction/1054681
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1-(2-(4-Bromophenoxy)ethyl)piperazine | HCID 23325337 | — |
| Edukt | methyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylate | HCID 86698665 | — |
| Katalysator | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Lösungsmittel | Toluene ethanol | HCID 21863594 | — |
| Produkt | methyl 6-chloro-5-{4-[2-(piperazin-1-yl)ethoxy]phenyl}-1H-indole-3-carboxylate | HCID 86698684 | 64,4% |
Reaktionsschritte
A mixture of methyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylate (80 mg, 0.15 mmol), 1-(2-(4-bromophenoxy)ethyl)piperazine (86 mg, 0.30 mmol), 2.0 M aqueous potassium carbonate (0.50 mL, 1.0 mmol), and Pd(dppf)Cl2 (10 mg, 0.01 mmol) in toluene/ethanol (1.44 mL/0.48 mL) was stirred at 110° C. for 2.5 hours. The mixture was poured into ethyl acetate and washed with water. The organic phase was dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue, which was purified by preparative TLC to give the title compound (40 mg, 40% yield) as a white solid. 1H NMR (400 MHz, CDCl3): δ8.50 (s, 1 H), 8.10 (s, 1 H), 7.98 (s, 1 H), 7.55 (m, 1 H), 7.45 (m, 2 H), 7.00 (m, 2 H), 4.20 (m, 2 H), 3.90 (s, 3 H), 2.99 (m, 4 H), 2.85 (m, 2 H), 2.60 (m, 4 H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09394285B2 |
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| Quelldatensatz | uspto-grants-2016_07 |
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| ORD ID | ord-3f60ca154ce5409697c81f8cb072bd13 |
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| Quellennotiz | uspto-grants-2016_07 |
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