反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([O:12][CH:13]2[CH2:17][CH2:16][N:15]([CH3:18])[C:14]2=[O:19])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].Cl.CN(C)CC(O)=O.I[C:29]1[CH:34]=[CH:33][C:32]([C:35]2[O:36][C:37]([CH3:40])=[N:38][N:39]=2)=[CH:31][CH:30]=1>O1CCOCC1.[Cu](I)I>[CH3:40][C:37]1[O:36][C:35]([C:32]2[CH:31]=[CH:30][C:29]([O:1][C:2]3[CH:3]=[C:4]([CH:9]=[C:10]([O:12][CH:13]4[CH2:17][CH2:16][N:15]([CH3:18])[C:14]4=[O:19])[CH:11]=3)[C:5]([O:7][CH3:8])=[O:6])=[CH:34][CH:33]=2)=[N:39][N:38]=1参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
To a stirred mixture of Methyl 3-hydroxy-5-(1-methyl-2-oxopyrrolidin-3-yloxy)benzoate (15 g) (Intermediate 3), N,N-dimethylglycine hydrochloride (2.3 g), copper (II) iodide (1 g) in dry 1,4-dioxane was added 2-(4-iodophenyl)-5-methyl-1,3,4-oxadiazole (15.4 g) (Intermediate 4) under nitrogen. The reaction mixture was refluxed for 24 h. The reaction mixture was cooled, quenched with water and extracted with DCM. Combined organic washings were washed with water, brine, dried over Na2SO4, filtered and concentrated in vacuo to get the crude product. The crude product was purified by column chromatography using silica gel as stationary phase and ethyl acetate: petroleum ether (9:1) as mobile phase to give the product (7 g) as thick liquid.
後処理
- temperatureThe reaction mixture was refluxed for 24 h
- temperatureThe reaction mixture was cooled
- customquenched with water
- extractionextracted with DCM
- washCombined organic washings were washed with water, brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto get the crude product
- customThe crude product was purified by column chromatography
出典と根拠
- ORDレコード
- ord-5e29f283917d45e2a7c3fd3018e4b0ee
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08835469B2
関連ノート
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