Reaktionsgleichung
[CH3:1][C:2]([O:7][CH2:8][C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]([CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[N:10]=1)([CH3:6])[C:3]([OH:5])=[O:4].Cl[CH:26]1[C:35]2C(=CC=CC=2)CC[CH2:27]1>>[CH3:6][C:2]([O:7][CH2:8][C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]([CH:18]2[C:19]3[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:35][CH2:26][CH2:27]2)[N:10]=1)([CH3:1])[C:3]([OH:5])=[O:4]Komponenten
3
Versuchsvorschrift
The product was prepared according to the procedure described in Example 6b), using as starting material 2-methyl-2-[(1-benzyl-1H-indazol-3-yl)methoxy]propanoic acid as starting material and 1-chloro-1,2,3,4-tetrahydronaphthalene as reagent.
Aufarbeitung
- customThe product was prepared
Quellen und Nachweise
- ORD-Eintrag
- ord-aae1fc72976c48e9973caadd6feac10c
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08835481B2
Verknüpfte Notizen
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