反応式
I[C:2]1[CH:7]=[CH:6][C:5]([C:8]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:9])=[CH:4][N:3]=1.[CH3:18][C:19]([CH3:31])([O:22][C:23]1[CH:30]=[CH:29][C:26]([C:27]#[N:28])=[CH:25][CH:24]=1)[C:20]#[CH:21]>C(NCC)C.[Cu]I.[Pd](Cl)Cl.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[C:27]([C:26]1[CH:29]=[CH:30][C:23]([O:22][C:19]([CH3:18])([CH3:31])[C:20]#[C:21][C:2]2[CH:7]=[CH:6][C:5]([C:8]([O:10][CH2:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[O:9])=[CH:4][N:3]=2)=[CH:24][CH:25]=1)#[N:28]参加物
7
反応物 2
生成物 1
試薬・触媒・溶媒 4
実験手順
12.2 g of benzyl 2-iodopyridine-5-carboxylate and 5.64 g of 4-(1,1-dimethyl-2-propynyloxy)benzonitrile were stirred with 32 mg of copper(I) iodide, 162 mg of triphenylphosphine and 180 mg of palladium(II) chloride in 280 ml of diethylamine at room temperature for 7 days under a nitrogen atmosphere. The mixture was evaporated and the residue was taken up in ethyl acetate and water. The organic phase was separated, dried over sodium sulphate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/petroleum ether (1:4) for the elution. There were obtained 9.04 g of benzyl 2-[3-(4-cyanophenoxy)-3-methyl-1-butyn-1-yl]pyridine-5-carboxylate which was used without further purification.
後処理
- customThe mixture was evaporated
- customThe organic phase was separated
- dry with materialdried over sodium sulphate
- customevaporated
- customThe residue was chromatographed on silica gel
- washfor the elution
出典と根拠
- ORDレコード
- ord-664c66a1d07b494b978510dba2f04462
- 出典データセット
- uspto-grants-1992_06
- 特許番号
- US05118694
関連ノート
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