6-(Piperidin-4-yl)-[1,2,4]triazolo[4,3-a]pyridine → 7-(Piperidin-4-yl)-[1,2,4]triazolo[4,3-a]pyridine
反応式
N1CCC(C2C=CC3N(C=NN=3)C=2)CC1.[N:16]1[N:17]=[CH:18][N:19]2[CH:24]=[CH:23][C:22]([CH:25]3[CH2:30][CH2:29][N:28](C(OC(C)(C)C)=O)[CH2:27][CH2:26]3)=[CH:21][C:20]=12.N1N=CN2C=C(C3CCN(C(OC(C)(C)C)=O)CC3)C=CC=12>>[NH:28]1[CH2:27][CH2:26][CH:25]([C:22]2[CH:23]=[CH:24][N:19]3[CH:18]=[N:17][N:16]=[C:20]3[CH:21]=2)[CH2:30][CH2:29]1参加物
4
反応物 3
生成物 1
実験手順
The title compound was prepared using standard chemical manipulations and procedures similar to those used for the preparation of compound 36.2, except tert-butyl 4-([1,2,4]triazolo[4,3-a]pyridin-7-yl)piperidine-1-carboxylate (compound 41.3) was used in place of tert-butyl 4-([1,2,4]thazolo[4,3-a]pyridin-6-yl)piperidine-1-carboxylate (compound 36.1) m/z (ES+) 203 (M+H)+.
出典と根拠
- ORDレコード
- ord-eb2b96d729554ce1b846748efe3d45df
- 出典データセット
- uspto-grants-2016_08
- 特許番号
- US09428502B2
反応ノート
読み込み中…