HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13144Erstellt: 23. Oktober 2026
Butyronitrile → 1-Methyl-2-phenyl-2-(1-pyridin-2-yl-1H-indazol-5-yloxy)-ethylamine
https://huagongshe.com/de/reaction/13144
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Butyronitrile | HCID 8008 | — |
| Edukt | Phenylpropanolamine | HCID 10297 | — |
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | 5-iodo-1-pyridin-2-yl-1H-indazole | HCID 59339792 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Produkt | 1-Methyl-2-phenyl-2-(1-pyridin-2-yl-1H-indazol-5-yloxy)-ethylamine | HCID 66812998 | 16,3% |
Reaktionsschritte
5-Iodo-1-pyridin-2-yl-1H-indazole (118b, 81 mg, 0.25 mmol), (1R,2S)-(−)-norephedrine (119 mg, 0.79 mmol) and butyronitrile (3 ml) were charged in a 7 ml vial. Copper(I) iodide (5.8 mg, 0.1 mol %) and cesium carbonate (261 mg, 0.8 mmol) were added, the vial was sealed and the solution was stirred (magnetic bar) at 125° C. for 2 h. Inorganic material was filtered off, and washed with ethyl acetate. The ethyl acetate phase was collected and concentrated and purified on silica with methanol:ethyl acetate 0:100 to 30:70 over 45 min. Pure fractions were pooled and concentrated to give 14 mg (16%) of 1-methyl-2-phenyl-2-(1-pyridin-2-yl-1H-indazol-5-yloxy)-ethylamine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07728030B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-e28520b5e84c42ad8fef41126721be9b |
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| Quellennotiz | uspto-grants-2010_06 |
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