6-Chloropyridine-2-carbonitrile → 6-((((2S,3R)-3-Methyl-1-(5-methyl-2-(2H-1,2,3-triazol-2-yl)benzoyl)piperidin-2-yl)methyl)amino)picolinonitrile

HRID 61010ノート

反応式

HRID 61010 の反応式
C[C@@H:2]1[CH2:7][CH2:6][CH2:5][N:4](C(C2C=C(C)C=CC=2C2C=NN(C)C=2)=O)[C@@H:3]1[CH2:23][NH:24]C1C=CC(C(F)(F)F)=CN=1.[NH2:35][CH2:36][C@@H:37]1[C@H:42]([CH3:43])[CH2:41][CH2:40][CH2:39][N:38]1[C:44]([C:46]1[CH:51]=[C:50]([CH3:52])[CH:49]=[CH:48][C:47]=1[N:53]1[N:57]=[CH:56][CH:55]=[N:54]1)=[O:45].ClC1N=C(C#N)C=CC=1>>[CH3:43][C@@H:42]1[CH2:41][CH2:40][CH2:39][N:38]([C:44](=[O:45])[C:46]2[CH:51]=[C:50]([CH3:52])[CH:49]=[CH:48][C:47]=2[N:53]2[N:57]=[CH:56][CH:55]=[N:54]2)[C@@H:37]1[CH2:36][NH:35][C:5]1[N:4]=[C:3]([C:23]#[N:24])[CH:2]=[CH:7][CH:6]=1

参加物

4

実験手順

The title compound was synthesized following the same general protocol as described for ((2S,3R)-3-methyl-2-(((5-(trifluoromethyl)pyridin-2-yl)amino)methyl)piperidin-1-yl)(5-methyl-2-(1-methyl-1H-pyrazol-4-yl)phenyl)methanone in Example A1, using ((2S,3R)-2-(aminomethyl)-3-methylpiperidin-1-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone and 6-chloropicolinonitrile. ESI-MS (m/z): 416 [M+1]+.

出典と根拠

ORDレコード
ord-19deecaf209f436b8ae9a11fe0c8a3e9
出典データセット
uspto-grants-2016_09
特許番号
US09440982B2

反応ノート

読み込み中…