Potassium Hydroxide → 6-(dimethylamino)-1H-indole-2-carboxylic acid
Reaktionsgleichung
[CH3:1][N:2]([C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]([O:15]C)=[O:14])[NH:10]2)=[CH:6][CH:5]=1)[CH3:3].[OH-].[K+]>>[CH3:3][N:2]([C:4]1[CH:12]=[C:11]2[C:7]([CH:8]=[C:9]([C:13]([OH:15])=[O:14])[NH:10]2)=[CH:6][CH:5]=1)[CH3:1]Komponenten
3
Versuchsvorschrift
Following the general procedure of PREPARATION 63 and making non-critical variations but starting with methyl 6-(N,N-dimethylamino)indole-2-carboxylate (PREPARATION 88, 0.80 g), potassium hydroxide (0.25 g), the title compound is obtained, NMR (300 MHz, CD3OD) 7.62, 7.13, 7.11, 7.01, and 3.11 δ.
Aufarbeitung
- customthe general procedure of PREPARATION 63
Quellen und Nachweise
- ORD-Eintrag
- ord-2a2183cb021549fb8816cb1dc407b928
- Quelldatensatz
- uspto-grants-1996_02
- Patentnummer
- US05489593
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