Hydrochloric Acid → HCID 71093241, Verbindung
Reaktionsgleichung
C(O)=O.[NH2:4][CH2:5][C@@H:6]([C:15]1[CH:24]=[CH:23][C:22]([OH:25])=[C:21]2[C:16]=1[CH:17]=[CH:18][C:19](=[O:26])[NH:20]2)[O:7][Si](C(C)(C)C)(C)C.[ClH:27]>CO>[ClH:27].[NH2:4][CH2:5][C@@H:6]([C:15]1[CH:24]=[CH:23][C:22]([OH:25])=[C:21]2[C:16]=1[CH:17]=[CH:18][C:19](=[O:26])[NH:20]2)[OH:7]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
(R)-5-(2-Amino-1-(tert-butyldimethylsilyloxy)ethyl)-8-hydroxyquinolin-2(1H)-one formate (0.23 g, 0.61 mmol) was dissolved in hydrochloric acid (5 mL, 4 M solution in dioxane) and methanol (5 mL). The reaction mixture was stirred at RT for 16 hours before concentrating in vacuo. The resulting residue was washed with ethyl acetate and dried in a vacuum oven for 18 hours to afford the title compound (0.15 g, 99%).
Aufarbeitung
- concentrationbefore concentrating in vacuo
- washThe resulting residue was washed with ethyl acetate
- customdried in a vacuum oven for 18 hours
Quellen und Nachweise
- ORD-Eintrag
- ord-80c7344e52664330819cc9616e1605df
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08877774B2
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