HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 876214Erstellt: 25. Oktober 2026
Acetonitrile → 3-Tetrahydrofuran-3-yl-3,8-diazabicyclo[3.2.1]octane
https://huagongshe.com/reaction/876214
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetonitrile | HCID 6342 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | tert-Butyl 4-(2-oxo-2,3-dihydro-1H-indol-1-yl)piperidine-1-carboxylate | HCID 67472855 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-Tetrahydrofuran-3-yl-3,8-diazabicyclo[3.2.1]octane | HCID 90414014 | 99% |
Reaktionsschritte
Tert-butyl 4-(2-oxoindolin-1-yl)piperidine-1-carboxylate (100 mg, 0.32 mmol) in ACN is cooled down to −10° C., N-bromosuccinimide (56.47 mg, 0.32 mmol) is added and stirred at −10° C. for 2 h. The reaction mixture is diluted with dichlormethane and water. The organic layer is separated, dried and concentrated. The crude product is used for the next step without further purification. Yield 99%, m/z 395 [M+H]+, rt 1.126 min, LC-MS Method Z020_S01.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08987249B2 |
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| Quelldatensatz | uspto-grants-2015_03 |
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| ORD ID | ord-da02d577f2cd441789b6783cfa870619 |
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| Quellennotiz | uspto-grants-2015_03 |
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