反応式
F[B-](F)(F)F.[C:6]([PH+](C(C)(C)C)C(C)(C)C)(C)(C)[CH3:7].C[Si](C#C)(C)C.Br[C:26]1[CH:27]=[CH:28][C:29]2[N:30]([C:32]([CH2:35][O:36][C:37]3[C:46]4[C:41](=[CH:42][C:43]([O:47][CH3:48])=[CH:44][CH:45]=4)[N:40]=[CH:39][CH:38]=3)=[N:33][N:34]=2)[CH:31]=1>O1CCOCC1.C(N(CC)CC)C.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].[Cu]I>[C:6]([C:26]1[CH:27]=[CH:28][C:29]2[N:30]([C:32]([CH2:35][O:36][C:37]3[C:46]4[C:41](=[CH:42][C:43]([O:47][CH3:48])=[CH:44][CH:45]=4)[N:40]=[CH:39][CH:38]=3)=[N:33][N:34]=2)[CH:31]=1)#[CH:7]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 4
反応条件
- 温度
- 80 °C
実験手順
Tri-t-butylphosphonium tetrafluoroborate (0.0377 g, 0.130 mmol), tris(dibenzylideneacetone)dipalladium (0.0594 g, 0.0649 mmol), trimethylsilyl acetylene (1.82 ml, 13.0 mmol), 4-((6-bromo-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methoxy)-7-methoxyquinoline (0.500 g, 1.30 mmol) were taken up in dioxane (10 mL) and triethylamine (3 mL). Added CuI. Sealed in a tube and heated at 80° C. for 3 h. Concentrated. Took up in MeOH and added solid potassium carbonate (large excess). Allowed to stir for 30 min. Filtered through a plug of Celite and concentrated. Took up in 10% MeOH in DCM and filtered through a plug of silica gel to afford 4-((6-ethynyl-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methoxy)-7-methoxyquinoline. MS m/z=331.0 [M+1]+. Calc'd for C19H14N4O2: 330.3.
後処理
- customSealed in a tube
- concentrationConcentrated
- additionadded solid potassium carbonate (large excess)
- filtrationFiltered through a plug of Celite
- concentrationconcentrated
- filtrationfiltered through a plug of silica gel
出典と根拠
- ORDレコード
- ord-9ee07d29b49a4cf8a703c00f9149bf69
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08524900B2
関連ノート
読み込み中…