Piperidine → 1-(Quinoxalin-6-ylcarbonyl)piperidine

HRID 442645

Reaktionsgleichung

Reaktionsgleichung von HRID 442645
[N:1]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([OH:13])=O)=[CH:8][CH:9]=2)[N:4]=[CH:3][CH:2]=1.[NH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1.C(C1NC=CN=1)(C1NC=CN=1)=O>>[N:1]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([N:14]3[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]3)=[O:13])=[CH:8][CH:9]=2)[N:4]=[CH:3][CH:2]=1

Komponenten

4

Versuchsvorschrift

The coupling of 6-quinoxalinecarboxylic acid to piperidine is accomplished in a manner similar to that used for the preparation of Invention Compound XIII, or by any other method known in the art for activation of aromatic carboxylic acids, such as, for example, activation by carbonyl diimidazole. 1H NMR δ 1.56 and 1.73 (br, 6), 3.40 (br s, 2), 3.79 (br s, 2), 7.82 (dd, 1, J=8.8, 1.9Hz), 8.13 (d, 1, J=1.6 Hz), 8.17 (d, 1, 8.6 Hz), and 8.9 ppm (m, 2).

Quellen und Nachweise

ORD-Eintrag
ord-10e3d0b07b8b4fd699e6754aa8a709f8
Quelldatensatz
uspto-grants-1999_04
Patentnummer
US05891876

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