Tetrabutylammonium Fluoride → 1-(2-Chloro-4-fluoro-phenyl)-2-(4-hydroxy-phenyl)-3-methyl-5-piperidin-yl-1,5,6,7-tetrahydro-pyrrolo[3,2-c]pyridin-4-one
反応式
[Si]([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[N:23]([C:24]3[CH:29]=[CH:28][C:27]([F:30])=[CH:26][C:25]=3[Cl:31])[C:22]3[CH2:21][CH2:20][N:19]([N:32]4[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]4)[C:18](=[O:38])[C:17]=3[C:16]=2[CH3:39])=[CH:11][CH:10]=1)(C(C)(C)C)(C)C.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1>[Cl:31][C:25]1[CH:26]=[C:27]([F:30])[CH:28]=[CH:29][C:24]=1[N:23]1[C:22]2[CH2:21][CH2:20][N:19]([N:32]3[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]3)[C:18](=[O:38])[C:17]=2[C:16]([CH3:39])=[C:15]1[C:12]1[CH:11]=[CH:10][C:9]([OH:8])=[CH:14][CH:13]=1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
2-[4-(tert-Butyldimethylsilanyloxy)phenyl]-1-(2-chloro-4-fluorophenyl)-3-methyl-5-piperidin-1-yl-1,5,6,7-tetrahydropyrrolo[3,2-c]pyridin-4-one (0.929 g, 1.63 mmol) was suspended in THF (10 ml) and TBAF (1 M in THF, 1.64 ml) was added. The reaction mixture was stirred at rt for 1 h whereafter the solvent was evaporated and ethyl acetate/water added. The phases were separated and the organic phase dried and evaporated. The crude product was recrystallised from ethyl acetate/toluene to yield the product as an orange solid (0.223 g, 23% over 3 steps).
後処理
- customwas evaporated
- additionethyl acetate/water added
- customThe phases were separated
- customthe organic phase dried
- customevaporated
- customThe crude product was recrystallised from ethyl acetate/toluene
出典と根拠
- ORDレコード
- ord-af9eb2a7fcd74155b54c1299c66eaed2
- 出典データセット
- uspto-grants-2009_08
- 特許番号
- US07576095B2
反応ノート
読み込み中…