Picolyl chloride hydrochloride → Methyl 5-(pyridin-2-ylmethoxy)-1H-indole-2-carboxylate
Reaktionsgleichung
Cl.Cl[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1.[OH:10][C:11]1[CH:12]=[C:13]2[C:17](=[CH:18][CH:19]=1)[NH:16][C:15]([C:20]([O:22][CH3:23])=[O:21])=[CH:14]2>>[N:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[CH2:3][O:10][C:11]1[CH:12]=[C:13]2[C:17](=[CH:18][CH:19]=1)[NH:16][C:15]([C:20]([O:22][CH3:23])=[O:21])=[CH:14]2Komponenten
3
Versuchsvorschrift
2-Chloromethylpyridine hydrochloride (515 mg) and methyl 5-hydroxy-1H-indole-2-carboxylate (600 mg) were processed in the same manner as in Production Example 1-1 to obtain the entitled compound (160 mg).
Quellen und Nachweise
- ORD-Eintrag
- ord-1300b71d4d044fc9aa10397a27f3c6f6
- Quelldatensatz
- uspto-grants-2009_07
- Patentnummer
- US07566781B2
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