Dimethylformamide → 5-(4-Fluorophenylethynyl)-pyridine-3-carbaldehyde
反応式
C([Mg]Cl)(C)C.[O:6]1CCC[CH2:7]1.Br[C:12]1[CH:13]=[N:14][CH:15]=[C:16]([C:18]#[C:19][C:20]2[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=2)[CH:17]=1.CN(C)C=O>>[F:26][C:23]1[CH:24]=[CH:25][C:20]([C:19]#[C:18][C:16]2[CH:17]=[C:12]([CH:7]=[O:6])[CH:13]=[N:14][CH:15]=2)=[CH:21][CH:22]=1参加物
5
実験手順
Prepare in a similar manner as described in EXAMPLE 90, using a 2 M solution of isopropylmagnesium chloride in tetrahydrofuran (2.99 mL, 5.98 mmol), 3-bromo-5-(4-fluorophenylethynyl)-pyridine (1.50 g, 5.43 mmol), (prepared essentially as described in EXAMPLE 96), and anhydrous N,N-dimethylformamide (1.99 g, 27.16 mmol) to give the title compound (0.29 g, 24%).
後処理
- customPrepare in a similar manner
- custom(prepared essentially
出典と根拠
- ORDレコード
- ord-0fbfbc71b9504dfcb13a38ab6e4b5497
- 出典データセット
- uspto-grants-2011_03
- 特許番号
- US07915424B2
反応ノート
読み込み中…