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

HRID 442645

反応式

HRID 442645 の反応式
[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

参加物

4

実験手順

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).

出典と根拠

ORDレコード
ord-10e3d0b07b8b4fd699e6754aa8a709f8
出典データセット
uspto-grants-1999_04
特許番号
US05891876

関連ノート

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