反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[F:9].[Li]CCCC.[C:15]([C:17]1[CH:37]=[CH:36][C:20]([O:21][C:22]2[CH:23]=[CH:24][C:25]([C:28]([F:35])([F:34])[C:29](OCC)=[O:30])=[N:26][CH:27]=2)=[CH:19][CH:18]=1)#[N:16]>C(OCC)C>[F:9][C:3]1[CH:4]=[C:5]([F:8])[CH:6]=[CH:7][C:2]=1[C:29](=[O:30])[C:28]([C:25]1[N:26]=[CH:27][C:22]([O:21][C:20]2[CH:19]=[CH:18][C:17]([C:15]#[N:16])=[CH:37][CH:36]=2)=[CH:23][CH:24]=1)([F:34])[F:35]参加物
実験手順
To a solution of 1-bromo-2,4-difluorobenzene (0.724 g, 3.77 mmol) in diethyl ether (Et2O)(20 mL) under a N2 atmosphere was added n-BuLi (2.49 mL, 4.03 mmol) at −78° C. and the reaction mixture was stirred for 45 minutes. Ethyl 2-(5-(4-cyanophenoxy)pyridin-2-yl)-2,2-difluoroacetate (1.00 g, 3.1 mmol) in Et2O (5 mL) was added dropwise and the reaction was stirred at the same temperature for 1 h. The reaction mixture was carefully quenched with 1N HCl until the reaction mixture was acidic. The reaction mixture was allowed to warm to room temperature and was extracted with Et2O. The combined organic phases were dried (Na2SO4) and concentrated to afford the title compound as yellow solid that was used for the next step without further purification (1.0 g, 83% crude yield): 1H NMR (300 MHz, CDCl3) δ 8.36 (d, J=2.7 Hz, 1H), 8.15-8.02 (m, 1H), 7.86 (d, J=8.7 Hz, 1H), 7.74-7.65 (m, 2H), 7.53 (dd, J=8.6, 2.7 Hz, 1H), 7.16-7.06 (m, 2H), 7.05-6.96 (m, 1H), 6.84 (ddd, J=10.9, 8.6, 2.4 Hz, 1H); 19F NMR (376 MHz, CDCl3) δ −99.13 (d, J=13.5 Hz), −100.67 (d, J=14.9 Hz), −101.82 (dd, J=28.5, 14.2 Hz); ESIMS m/z 387 ([M+1]+).
後処理
- stirringthe reaction was stirred at the same temperature for 1 h
- customThe reaction mixture was carefully quenched with 1N HCl until the reaction mixture
- extractionwas extracted with Et2O
- dry with materialThe combined organic phases were dried (Na2SO4)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-41456b0e4da845108fff41fe16983756
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09447073B2
関連ノート
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