反応式
Cl[C:2]([F:7])([F:6])C([O-])=O.[Na+].Br.[CH3:10][C:11]1[CH:15]=[C:14]([C:16]2[CH:17]=[CH:18][C:19]3[N:20]([C:22]([CH2:25][O:26][C:27]4[C:36]5[C:31](=[CH:32][C:33]([OH:37])=[CH:34][CH:35]=5)[N:30]=[CH:29][CH:28]=4)=[N:23][N:24]=3)[CH:21]=2)[O:13][N:12]=1.C(=O)([O-])[O-].[Cs+].[Cs+].CN(C=O)C>C(O)=O>[F:7][CH:2]([F:6])[O:37][C:33]1[CH:32]=[C:31]2[C:36]([C:27]([O:26][CH2:25][C:22]3[N:20]4[CH:21]=[C:16]([C:14]5[O:13][N:12]=[C:11]([CH3:10])[CH:15]=5)[CH:17]=[CH:18][C:19]4=[N:24][N:23]=3)=[CH:28][CH:29]=[N:30]2)=[CH:35][CH:34]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
A 48 mL tube was charged with sodium 2-chloro-2,2-difluoroacetate (0.15 g, 1.0 mmol), 4-((6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methoxy)quinolin-7-ol hydrobromide (0.200 g, 0.44 mmol), cesium carbonate (0.43 g, 1.3 mmol), and DMF (1.7 ml, 22 mmol), flushed with argon, sealed, then placed in a 100° C. oil bath for 5 hours. The reaction mixture was concentrated, then diluted with DCM and chloroform. This was washed with water, sat. NaHCO3, and brine, then dried with MgSO4, filtered, and concentrated to give a brown oil. This was purified by HPLC to give 7-(difluoromethoxy)-4-((6-(3-methylisoxazol-5-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)methoxy)quinoline (0.025 g, 13% yield) as the formic acid salt. MS (ESI pos. ion) m/z: 424 (MH+). Calc'd exact mass for C21H15F2N5O3: 423.
後処理
- customflushed with argon
- customsealed
- customplaced in a 100° C.
- customfor 5 hours
- concentrationThe reaction mixture was concentrated
- additiondiluted with DCM and chloroform
- washThis was washed with water, sat. NaHCO3, and brine
- dry with materialdried with MgSO4
- filtrationfiltered
- concentrationconcentrated
- customto give a brown oil
- customThis was purified by HPLC
出典と根拠
- ORDレコード
- ord-3c483852cdbc403497b1e754dee62bb0
- 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…