Diisopropylamine → Ethyl 1-(4-fluorophenyl)-2-((2-(trifluoromethyl)phenyl)ethynyl)-1H-imidazole-5-carboxylate
反応式
Cl[C:2]1[CH:7]=[CH:6][CH:5]=[C:4](F)[C:3]=1[C:9]#[C:10][C:11]1[N:12]([C:21]2[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=2)[C:13]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:14][N:15]=1.FC1C=CC(N2C(C(OCC)=O)=CN=C2I)=CC=1.C(C1C=CC=CC=1[C:54]([F:57])([F:56])[F:55])#C.C(NC(C)C)(C)C>Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[Cu]I.C1COCC1>[F:27][C:24]1[CH:23]=[CH:22][C:21]([N:12]2[C:13]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[CH:14][N:15]=[C:11]2[C:10]#[C:9][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[C:54]([F:57])([F:56])[F:55])=[CH:26][CH:25]=1参加物
8
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
Ethyl 1-(4-fluorophenyl)-2-((2-(trifluoromethyl)phenyl)ethynyl)-1H-imidazole-5-carboxylate (46) was prepared in a similar manner as that described for the synthesis of compound 42 using ethyl 1-(4-fluorophenyl)-2-iodo-1H-imidazole-5-carboxylate (38) (900 mg, 2.5 mmol), 1-ethynyl-2-(trifluoromethyl)benzene (0.42 mL, 3.0 mmol), PdCl2(PPh3)2 (88 mg, 0.13 mmol), copper (I) iodide (23 mg, 0.13 mmol), diisopropyl amine (7 mL), and THF (50 mL).
出典と根拠
- ORDレコード
- ord-93a1d828a72848ffb78bbdd6e2b7b112
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08703776B2
反応ノート
読み込み中…