1-Aminopiperidine → 6-Cyclohexyl-pyridine-2-carboxylic acid piperidin-1-ylamide
Reaktionsgleichung
[CH:1]1([C:7]2[N:12]=[C:11]([C:13]([OH:15])=O)[CH:10]=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[N:16]1([NH2:22])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1>>[N:16]1([NH:22][C:13]([C:11]2[CH:10]=[CH:9][CH:8]=[C:7]([CH:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)[N:12]=2)=[O:15])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1Komponenten
3
Versuchsvorschrift
The title compound was synthesized in analogy to Example 1, using 6-cyclohexyl-pyridine-2-carboxylic acid (Example 7 b) and 1-piperidinamine (CAN 2213-43-6) as starting materials, MS (EI): 288.3 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-f5d778ff018140d2b857f9962a5216ad
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09290451B2
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