6-(3-Methyl-5-pyridin-2-yl-3H-[1,2,3]triazol-4-ylmethoxy)-nicotinic acid → 6-[5-(5-Fluoro-pyridin-2-yl)-3-methyl-3H-[1,2,3]triazol-4-ylmethoxy]-N-(tetrahydro-pyran-4-yl)-nicotinamide
反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[N:12]=[N:11][N:10]([CH3:13])[C:9]=2[CH2:14][O:15][C:16]2[CH:24]=[CH:23][C:19]([C:20]([OH:22])=O)=[CH:18][N:17]=2)=[N:6][CH:7]=1.CN1[C:30]([CH2:31][O:32]C2C=CC(C(O)=O)=CN=2)=[C:29]([C:42]2[CH:47]=CC=CN=2)[N:28]=N1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[N:12]=[N:11][N:10]([CH3:13])[C:9]=2[CH2:14][O:15][C:16]2[CH:24]=[CH:23][C:19]([C:20]([NH:28][CH:29]3[CH2:30][CH2:31][O:32][CH2:47][CH2:42]3)=[O:22])=[CH:18][N:17]=2)=[N:6][CH:7]=1参加物
3
反応物 2
生成物 1
実験手順
As described for example 26b, 6-[5-(5-fluoro-pyridin-2-yl)-3-methyl-3H-[1,2,3]triazol-4-ylmethoxy]-nicotinic acid (82 mg, 0.25 mmol), instead of 6-(3-methyl-5-pyridin-2-yl-3H-[1,2,3]triazol-4-ylmethoxy)-nicotinic acid, was converted to the title compound (80 mg, 78%) which was obtained as a white solid. MS: m/e=413.4 [M+H]+.
出典と根拠
- ORDレコード
- ord-1bd765fd9f124463a180cc5d4f835fe3
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08742097B2
反応ノート
読み込み中…