HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10560Erstellt: 24. Oktober 2026
Water → 4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine
https://huagongshe.com/de/reaction/10560
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | 4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine | HCID 21979972 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 4-(4-Methoxy-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine | HCID 21979974 | — |
Reaktionsschritte
A suspension of Intermediate 71 (600 mg) and copper(I) iodide (141 mg, Kanto Chemicals) in methanol (5.5 ml) and pyridine (5.5 ml) was added with sodium methoxide (28% methanol solution, 1.7 ml, Wako Pure Chemical Industries) and stirred with heating at 65° C. for 24 hours. The reaction mixture was cooled to room temperature, then added with water (30 ml) and extracted three times with ethyl acetate (20 ml for each time). The combined organic layer was washed twice with saturated brine (30 ml for each time) and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:2) to obtain the title compound (364 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07094789B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-e66b85a64f8c49938e94e99c298be080 |
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| Quellennotiz | uspto-grants-2006_08 |
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