Reaktionsgleichung
[O:1]1[C:5]2([CH2:10][CH2:9][C:8](C3C4C(=CC=CC=4)C(=O)N3C)=[CH:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.Br[C:23]1[CH:31]=[CH:30][C:29]([N+:32]([O-:34])=[O:33])=[C:28]2[C:24]=1[CH2:25][N:26]([CH3:36])[C:27]2=[O:35].O1C2(CCC(B3OC(C)(C)C(C)(C)O3)=CC2)OCC1>>[O:1]1[C:5]2([CH2:10][CH2:9][C:8]([C:23]3[CH:31]=[CH:30][C:29]([N+:32]([O-:34])=[O:33])=[C:28]4[C:24]=3[CH2:25][N:26]([CH3:36])[C:27]4=[O:35])=[CH:7][CH2:6]2)[O:4][CH2:3][CH2:2]1Komponenten
4
Edukt 3
Produkt 1
Versuchsvorschrift
The title product was prepared according to the procedure for 7-amino-4-(1,4-dioxaspiro[4,5]dec-7-ene-8-yl-2-methyl-2,3-dihydro-1H-isoindol-1-one using 4-bromo-2-methyl-7-nitro-2,3-dihydro-1H-isoindol-1-one and 1,4-dioxaspiro[4,5]dec-7-ene-8-boronic acid pinacol ester.
Quellen und Nachweise
- ORD-Eintrag
- ord-72ed046144b6454f898c7e943b66f07e
- Quelldatensatz
- uspto-grants-2015_08
- Patentnummer
- US09096624B2
Verknüpfte Notizen
Wird geladen…