4-Chloro-6-methylpyridine-2-carboxylic acid → HCID 70663423, Verbindung
Reaktionsgleichung
[CH3:1][NH:2][C:3]1[CH:4]=[N:5][CH:6]=[CH:7][C:8]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH3:15].[Cl:16][C:17]1[CH:22]=[C:21]([CH3:23])[N:20]=[C:19]([C:24](O)=[O:25])[CH:18]=1>>[CH3:1][N:2]([C:3]1[CH:4]=[N:5][CH:6]=[CH:7][C:8]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH3:15])[C:24]([C:19]1[CH:18]=[C:17]([Cl:16])[CH:22]=[C:21]([CH3:23])[N:20]=1)=[O:25]Komponenten
3
Versuchsvorschrift
The title compound was prepared in analogy to example 90, from N-methyl-4-o-tolylpyridin-3-amine (example 1, intermediate a) and 4-chloro-6-methylpyridine-2-carboxylic acid (CAS RN 30235-19-9). Colorless solid (35%). MS (ESI): m/z=352.12 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-1e1283c8e6a34babbcbf42c277c08b16
- Quelldatensatz
- uspto-grants-2015_03
- Patentnummer
- US08987307B2