5-chloro-1H-indole-2,3-dione → (3S,4R)-4-(5-Chloro-2,3-dioxo-2,3-dihydro-indol-1-yl)-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrile
Reaktionsgleichung
[CH3:1][C:2]1([CH3:15])[O:11][C:10]2[C:5](=[CH:6][C:7]([C:12]#[N:13])=[CH:8][CH:9]=2)[C@@H:4]2[O:14][C@H:3]12.[Cl:16][C:17]1[CH:18]=[C:19]2[C:23](=[CH:24][CH:25]=1)[NH:22][C:21](=[O:26])[C:20]2=[O:27]>>[Cl:16][C:17]1[CH:18]=[C:19]2[C:23](=[CH:24][CH:25]=1)[N:22]([C@@H:4]1[C:5]3[C:10](=[CH:9][CH:8]=[C:7]([C:12]#[N:13])[CH:6]=3)[O:11][C:2]([CH3:15])([CH3:1])[C@H:3]1[OH:14])[C:21](=[O:26])[C:20]2=[O:27]Komponenten
3
Versuchsvorschrift
Following the procedure described in the Example 1, using (S,S)-2,2-dimethyl-1a,7b-dihydro-2H-1,3-dioxa-cyclopropa[a]naphthalene-6-carbonitrile and 5-chloro-1H-indole-2,3-dione as starting materials, the title compound was prepared as a white solid.
Quellen und Nachweise
- ORD-Eintrag
- ord-0a80f1104ff94b6ca41c6f0ba6ea0bf7
- Quelldatensatz
- uspto-grants-2010_10
- Patentnummer
- US07812183B2
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